SpineGuard and XinRong Medical Group Sign Exclusive Distribution Agreement For PediGuard® in China

June 21, 2017

PARIS & SAN FRANCISCO–(BUSINESS WIRE)–Regulatory News:

SpineGuard (Paris:ALSGD) (FR0011464452 – ALSGD), an innovative company that develops and markets disposable medical devices designed to make spine surgery safer, announced today an exclusive distribution agreement with XinRong Medical Group for PediGuard® in China, Hong Kong and Macau.

China’s spine market has become the world’s second-largest market after the USA and is expected to be worth over $1 billion by 20191, driven by an aging population, increasing disease prevalence and treatment rates, along with growing affordability.

We are excited about this agreement and believe that XinRong Medical Group has all of the right attributes to successfully introduce PediGuard® in China, a market with great commercial potential. The number of spine fusions continues to grow rapidly across the country creating a substantial need for an easy-to-use smart device to secure the placement of pedicle screws consistently. Since its clearance by CFDA, numerous Chinese orthopedists and neurosurgeons have expressed a strong interest for our DSG™ technology. We now very much look forward to seeing them adopt it in their spine surgery practice,” said Pierre Jérôme, CEO and co-founder of SpineGuard.

“XR Medical is delighted to partner with SpineGuard, the company that owns PediGuard® and DSG™ technology. PediGuard® is the only one of its kind, and XinRong Medical is very excited to introduce one of the most advanced surgical solutions globally to the China market. SpineGuard’s cutting-edge technology allows surgical staff and patients to significantly reduce exposure to surgical radiation in the operating room while helping surgeons achieve more precise spinal implantation in real time. Ease of use, cost effectiveness, accuracy, and safety are the benefits that we want to bring to surgeons in China, through which we will continue to realize our vision of putting patients first,” added Christine Zhang, XinRong Medical Group’s CEO.

Next financial press release: 2017 Half-year revenue: July 6, 2017

About SpineGuard®
Founded in 2009 in France and the USA, by Pierre Jérôme and Stéphane Bette, SpineGuard’s mission is to make spine surgery safer by bringing real-time digital technology into the operating room. Its primary objective is to establish its proprietary DSG™ (Dynamic Surgical Guidance) technology as the global standard of surgical care, starting with safer screw placement in spine surgery and then in other surgeries. PediGuard®, the first device designed using DSG, was co-invented by Maurice Bourlion, Ph.D., Ciaran Bolger, M.D., Ph.D., and Alain Vanquaethem, Biomedical Engineer. It is the world’s first and only handheld device capable of alerting surgeons to potential pedicular or vertebral breaches. Over 50,000 surgical procedures have been performed worldwide with DSG™ enabled devices. Numerous studies published in peer-reviewed medical and scientific journals have demonstrated the multiple benefits that PediGuard® delivers to patients, surgical staff and hospitals. SpineGuard is expanding the scope of its DSG™ platform through strategic partnerships with innovative medical device companies and the development of smart instruments and implants. SpineGuard has offices in San Francisco and Paris. For further information, visit www.spineguard.com.

About XinRong Medical Group
XinRong Medical Group, a leader in medical technology, is dedicated to increasing patient affordability and providing the most advanced solutions for surgeons such that they can deliver the best patient care. XinRong Medical offers innovative solutions in orthopedic surgery, neurosurgery, reconstructive surgery, and minimally invasive therapy. Established in 2000 in Jiangsu Province, China, XinRong Medical was one of the first companies in China cleared by CFDA to manufacture Orthopedic Implants. In 2014, the Company received a strategic investment from The Blackstone Group (NYSE: BX). For additional information about XinRong Medical, please refer to our website www.XRBest.Com, or contact us directly at +86-512-58100828 or info@xrmed.com.

Disclaimer
The SpineGuard securities may not be offered or sold in the United States as they have not been and will not be registered under the Securities Act or any United States state securities laws, and SpineGuard does not intend to make a public offer of its securities in the United States. This is an announcement and not a prospectus, and the information contained herein does and shall not constitute an offer to sell or the solicitation of an offer to buy, nor shall there be any sale of the securities referred to herein in the United States in which such offer, solicitation or sale would be unlawful prior to registration or exemption from registration.

1 according to IData Research

Contacts

SpineGuard
Manuel Lanfossi, +33 (0)1 45 18 45 19
Chief Financial Officer
m.lanfossi@spineguard.com
or
Europe / NewCap
Investor Relations & Financial Communication
Florent Alba / Pierre Laurent, +33 (0)1 44 71 94 94
spineguard@newcap.fr
or
US
Ronald Trahan Associates Inc.
Ronald Trahan, APR, +1-508-359-4005, x108

Medicrea Announces Capital Raise of € 13 Million Through a Successful Private Placement

June 19, 2017

LYON, France & NEW YORK–(BUSINESS WIRE)–The Medicrea Group (ISIN : FR0004178572 – ALMED, eligible to PEA-PME), pioneering the convergence of healthcare IT and next-generation, outcome-centered device design and manufacturing with UNiD™ ASI technology, announced today the successful capital increase for the benefit of a specific category of beneficiaries through the accelerated construction of an order book.

Due to strong investor demand, the Company issued 2,680,413 new shares with a nominal value of € 0.16 per unit, at a unit price of € 4.85, including issue premium, for a total amount of € 13 million, compared to approximately € 10 million originally planned, representing 21.08% of the Company’s share capital after the transaction (the ‘Action’).

As an indication, the participation of a shareholder holding 1% of the share capital of the Company prior to the issue will become 0.79%.

The funds will be raised from international funds and / or investment companies carrying out multinational financial transactions in several, in support of Medicrea’s efforts:

1 / To accelerate the development, mainly in the United States, of the UNiD™ ASI platform to enable the Company to strengthen its position as a pioneer and world leader in personalized spinal technology, which includes comprehensive analytical services and biomechanical expertise for the collection and modeling of clinical data and the realization of patient-specific spinal implants; and

2 / To prepare for the commercialization of a new range of 3D-printed titanium interbody cages in the United States and Europe in preparation of pending regulatory clearances and sales agreements.

The proceeds of the capital increase associated with the current liquidity available should enable the Company to meet its future financial commitments over the next 18 months.

The Action was implemented by decision of the Board of Directors on 15 June, 2017 and the Chairman and Chief Executive Officer on 16 June, 2017, pursuant to the 9th Resolution approved by of the Combined Shareholders’ Meeting of May 11, 2017, at a price representing a discount of 9.94% compared to the volume-weighted average of the last twenty trading days preceding the decision of the Chief Executive Officer (€ 5.35) and 4.53% compared to the closing price of June 16, 2017 (€ 5.08).

The capital increase is carried out through the issuance of ordinary shares without preferential subscription rights in favor of a category of beneficiaries. The settlement of the new shares issued in connection with the capital increase and their admission to the Euronext Growth Paris exchange with Euronext Paris is scheduled for June 22, 2017. The new shares will bear current rights and will be admitted to trading on the Euronext Growth Paris exchange under ISIN code FR0004178572 – ALMED. The share capital of Medicrea will comprise 12,713,480 shares at the end of the settlement period. Thus, after the capital increase, the Company’s share capital has significantly changed. Post transaction, the holding of Orchard International and its executives is 19.17% of the total capital and the free float is 80.83%.

Midcap Partners acts as Lead Partner & Bookrunner of the Action.

EuroLand Corporate acted as a consultant to the Company.

In accordance with the provisions of Article 211-3 of the General Regulation of the AMF (Autorité des Marchés Financiers), the offer of the Company’s shares in connection with this capital increase for the benefit of a specific category of beneficiaries did not give rise to a submitted prospectus for the approval of the AMF. Detailed information about the Company, including its business activities, results and related risk profile, can be found in the Annual Financial Report for the year ended December 31, 2016, which is available for consultation, as well as other regulated information including press releases, on the Company’s website (www.medicrea.com).

Next financial publication: Sales for the 1st half of 2017: July 11, 2017, after market.

About Medicrea (www.Medicrea.com)

Through the lens of predictive medicine, Medicrea leads the design, integrated manufacture, and distribution of 30+ FDA approved implant technologies, utilized in over 100k spinal surgeries to date. Operating in a $10 billion marketplace, Medicrea is an SME with 175 employees worldwide, which includes 55 at its USA Corp. subsidiary in NYC. The Company has an ultra-modern manufacturing facility in Lyon, France housing the development and production of 3D-printed titanium patient-specific implants.

By leveraging its proprietary software analysis tools with big data and machine learning technologies supported by an expansive collection of clinical and scientific data, Medicrea is well-placed to streamline the efficiency of spinal care, reducing procedural complications and limiting time spent in the O.R.

For further information, please visit: www.medicrea.com.

Connect with Medicrea:
FACEBOOK | INSTAGRAM | TWITTER | WEBSITE | YOUTUBE

Medicrea is listed on
EURONEXT Growth Paris
ISIN: FR 0004178572
Ticker: ALMED

Caution

This press release is for informational purposes only. This press release does not constitute and cannot be regarded as an offer for public subscription or a solicitation of an interest in the public offering of financial securities. Dissemination of this press release in certain countries may constitute a violation of the legal provisions in force. The information contained in this press release does not constitute an offer of securities in France, the United States, Canada, Australia, Japan or any other country.

Contacts

The Medicrea Group
Denys Sournac
Founder, Chairman and CEO
dsournac@medicrea.com
or
Fabrice Kilfiger
Chief Financial Officer
fkilfiger@medicrea.com
Tel. : +33 (0)4 72 01 87 87

Kuros receives CE certification for Neuroseal®, a novel dural sealant

Schlieren (Zurich), Switzerland, June 21, 2017 – Kuros Biosciences (SIX:KURN) announced today that it has received CE certification for its novel dural sealant, Neuroseal® . The CE certification allows for the commercialization of the product anywhere in the European Economic Area. As part of the supporting evidence, Neuroseal® has been tested clinically and demonstrated effective sealing. Furthermore, Neuroseal® is specifically designed for ease of preparation, use and handling thereby reducing the risk of adverse effects which may result in longer hospitalizations and an increase in healthcare costs. With this approval and together with MagnetOsTM, Kuros has now two products ready to be commercialized in Europe.

The Conformité Européene (CE) mark allows Kuros to sell Neuroseal® , a Class III medical device, in all 27 member states of the European Union, the three countries of the European Free Trade Association (EFTA) plus Switzerland and Turkey. The CE certification testifies that Neuroseal® has been assessed to meet stringent regulatory requirements. The receipt of the CE approval involved a comprehensive audit of Kuros’ quality system and a thorough conformity assessment of Neuroseal® to assure that the product performs safely and as designed. As a result of the CE certification, Kuros is eligible for receiving a payment of USD 533, 000.

Dr. Ivan Cohen-Tanugi, Chief Executive Officer of Kuros, commented: “Today’s CE approval means that the entire European market is now open for us to commercially distribute Neuroseal® . The CE certification is another significant milestone as we continue to deliver on promises made. With Neuroseal® and MagnetOsTM, our portfolio now consists of two approved and commercial-stage products.” He continued: “Neuroseal® ensures watertight closure of the dura following brain surgery. It reduces the risk of postoperative leakage thereby improving quality of life of patients while also reducing hospitalizations costs. We believe the clinically proven advantages of Neuroseal® could make it the preferred option for physicians, patients, and payers.”

Neuroseal® effectively seals the dura reducing the risk of infections

Neuroseal® is a novel sealant designed as an adjunct to suturing to seal the dura after cranial surgery. The dura is a membrane surrounding the brain and spine and separates the central nervous system from the rest of the body. The dura acts as a protective barrier and ensures that the brain and spinal cord are bathed in cerebrospinal fluid (CSF), which is essential for the healthy functioning of the central nervous system. Amongst other functions it serves as cushion for the brain and protects against physical impacts and infections. During cranial procedures in which the dura is incised, the watertight closure is compromised, potentially leading to postoperative CSF leakage. CSF leakage may lead to clinical symptoms, neurological complications, and increased risk of infection. This may result in longer or recurrent periods of hospitalizations and associated increase in healthcare costs. Hence, there is a clear medical need to reduce the risk of CSF leakage after cranial surgery in which the dura is compromised.

Neuroseal® contains two synthetic polymers that are applied via a hand-spray device. The two polymers cross-link at the site of application to form a gel that seals the suture line. Results from a European clinical trial support Neuroseal® ’s safety and effectiveness. All clinical end-points were met with no safety issues observed.

For further information, please contact:

Kuros Biosciences Ltd

Harry Welten, Chief Financial Officer

Phone +41 79 750 15 64

harry.welten@kuros.ch

About Kuros Biosciences Ltd

Kuros Biosciences is focused on the development of innovative products for tissue repair and regeneration and is located in Schlieren (Zurich), Switzerland. The Company is listed according to the International Financial Reporting Standard on the SIX Swiss Exchange under the symbol KURN. Visit www.kuros.ch for additional information on Kuros, its science and product pipeline.

Forward Looking Statements

This media release contains certain forward-looking statements that involve risks and uncertainties that could cause actual results to be materially different from historical results or from any future results expressed or implied by such forward-looking statements. You are urged to consider statements that include the words “will” or “expect” or the negative of those words or other similar words to be uncertain and forward-looking. Factors that may cause actual results to differ materially from any future results expressed or implied by any forward-looking statements include scientific, business, economic and financial factors, Against the background of these uncertainties, readers should not rely on forward-looking statements. The Company assumes no responsibility for updating forward-looking statements or adapting them to future events or developments.

 

Kuros Biosciences Ltd, Wagistrasse 25, CH-8952 Schlieren

EIT Emerging Implant Technologies Moves Toward Commercialization of its 3D Printed Cellular Titanium Implants in the United States

Emerging Implant Technologies GmbH (EIT), a German medical device manufacturer exclusively focused on creating innovative technologies for spinal application by utilizing additive manufacturing, announces major milestones in preparation of its expected 510(k) approval later this year. EIT Cellular Titanium® is a porous titanium structure that has been designed according to scientific insights on ideal pore shape and size to optimize bone ingrowth. Due to the availability of Selective Laser Melting (SLM) technology and post-processing methods, it has been possible to create a highly porous, osteo-influential titanium scaffold for osseointegration. This EIT Cellular Titanium® structure has been applied in the complete ALIF, TLIF, PLIF and Cervical implant line, and clinical case studies and retrieval analysis demonstrate extensive bone ingrowth throughout the total implants in the cervical and lumbar spine in a short time frame.

To prepare for the launch of its innovative cellular titanium interbody devices, EIT has completed 3 major milestones. First, EIT has created a subsidiary and located its US Headquarters in Atlanta, GA. This move demonstrates its commitment to the US marketplace.

The second step EIT has made towards commercialization is by engaging GlobalMed Logistix (GMLx) to support its US distributors and surgeons by providing Warehousing, Supply Chain, Inventory Management and Customer Service. GlobalMed Logistix is a third-party logistics (3PL) company born from a rich 35-year distribution and warehousing history that will help coordinate and efficiently manage EIT’s logistics in the US.

Lastly, to help with Market Knowledge and Access, EIT has engaged Ortho Sales Partners (OSP). The primary areas of service that will be provided by OSP to EIT is Surgeon Access, Distributor Recruitment and Onboarding, Hospital Approvals and National Contracts through Group Purchasing Organizations (GPO) an Integrated Delivery Networks (IDN). Armed with the experience of the top industry talent, OSP leverages its team to help its clients shorten the cycle from launch to revenue.

Guntmar Eisen, Co-Founder and CEO for EIT says “We are very pleased to be partnered with these organizations in advance of our anticipated FDA Approval to help us deliver these innovative implants to US surgeons and patients. Our implants offer a combination of solid and cellular implant architecture to facilitate the rebuilding of natural cortical and cancellous bone structures while maintaining excellent imaging characteristics and we are eager to get started with our commercialization process.”

______

About EIT

EIT is the first medical device manufacturer to exclusively focus on spinal implants that are  designed according to latest published science on optimal bone ingrowth in porous titanium scaffolds and produced with additive manufacturing methods.

The EIT implants are made of EIT Cellular Titanium®, that addresses the clinical shortcomings of the current cage designs and materials (non-fusion, biocompatibility, subsidence, migration and imaging distortion), thereby obtaining very promising fusion results and improved clinical outcome due to the qualities of the porous 3-D printing of titanium. The highly porous titanium scaffold ensures extensive bone ingrowth as a result of its specific design and elasticity close to the cancellous bone. The limited amount of titanium material in the EIT implant ensures uncompromised imaging on X-ray and MRI and enabling excellent follow up on defining bone ingrowth and fusion with CT.

A complete portfolio of Smart Spinal Implants™ based on EIT Cellular Titanium® is available for the cervical and lumbar spine, with an extensive choice in footprint sizes, heights and lordosis angles to address the various anatomical requirements.  Over 10.000 cases have been performed in over 15 markets globally since 2014.

###

K2M Introduces First-of-Its-Kind SAHARA™ AL Expandable Stabilization System

LEESBURG, Va., June 20, 2017 (GLOBE NEWSWIRE) — K2M Group Holdings, Inc. (NASDAQ:KTWO) (the “Company” or “K2M”), a global leader of complex spine and minimally invasive solutions focused on achieving three-dimensional Total Body Balance, today announced the introduction of the SAHARA AL Expandable Stabilization System, the Company’s first expandable offering within its interbody portfolio. SAHARA AL is the only lordotic expandable interbody device with integrated screw fixation on the market to help achieve spinal balance.

The SAHARA AL Expandable Stabilization System represents a technological advancement over static interbody options, allowing for in-situ lordotic adjustment to match a patient’s sagittal profile through one fusion device. SAHARA AL is a zero-profile device with multi-screw fixation, designed to provide stability to the anterior column, while featuring a comprehensive range of lordotic adjustments of up to 26 degrees. It is indicated as a standalone device for lordotic angles of 15 degrees or less. SAHARA AL is manufactured from commercially pure grade II titanium, titanium alloy, and cobalt chrome.

“The anterior-lumbar interbody fusion (ALIF) approach allows for greater segmental lordosis correction and implant fixation than other alternative interbody approaches,” said Christopher Good, MD, FACS an orthopedic surgeon and Director of Scoliosis and Spinal Deformity at The Virginia Spine Institute in Reston, Virginia. “With variable in-situ lordotic adjustment, the SAHARA AL implant helps achieve sagittal balance and segmental reduction not generally attainable by ALIF cages with fixed lordotic angles.”

SAHARA AL features K2M’s innovative tifix® Locking Technology, which offers benefits such as allowing repeated screw adjustment up to three times, without compromising the locking feature. In addition, SAHARA AL features a comprehensive offering of footprints and heights to best fit patient anatomy.

“The introduction of the SAHARA AL Expandable Stabilization System marks a significant addition to our interbody portfolio as our first expandable offering in this category and the only device of its kind on the market today,” said Eric Major, President and CEO of K2M. “This latest milestone—coupled with the launch of our comprehensive, next-generation Balance ACS platform earlier this year—further reinforces our commitment to developing differentiated technologies with the goal of facilitating Total Body Balance.”

Balance ACS (BACS) is a comprehensive platform applying three-dimensional solutions across the entire clinical care continuum to help drive quality outcomes in spine patients. BACS provides solutions focused on achieving balance of the spine by addressing each anatomical vertebral segment with a 360-degree approach to the axial, coronal, and sagittal planes, emphasizing Total Body Balance as an important component of surgical success.

For more information on the SAHARA AL Expandable Stabilization System and K2M’s complete product portfolio, visit www.K2M.com. For more information about Balance ACS, visit www.BACS.com.

About K2M

K2M Group Holdings, Inc. is a global leader of complex spine and minimally invasive solutions focused on achieving three-dimensional Total Body Balance. Since its inception, K2M has designed, developed, and commercialized innovative complex spine and minimally invasive spine technologies and techniques used by spine surgeons to treat some of the most complicated spinal pathologies. K2M has leveraged these core competencies into Balance ACS, a platform of products, services, and research to help surgeons achieve three-dimensional spinal balance across the axial, coronal, and sagittal planes, with the goal of supporting the full continuum of care to facilitate quality patient outcomes. The Balance ACS platform, in combination with the Company’s technologies, techniques, and leadership in the 3D-printing of spinal devices, enable K2M to compete favorably in the global spinal surgery market. For more information, visit www.K2M.com and connect with us on Facebook, Twitter, Instagram, LinkedIn, and YouTube.

Forward-Looking Statements

This press release contains forward-looking statements that reflect current views with respect to, among other things, operations and financial performance.  Forward-looking statements include all statements that are not historical facts such as our statements about our expected financial results and guidance and our expectations for future business prospects.  In some cases, you can identify these forward-looking statements by the use of words such as “outlook,” “guidance,” “believes,” “expects,” “potential,” “continues,” “may,” “will,” “should,” “could,” “seeks,” “predicts,” “intends,” “plans,” “estimates,” “anticipates” or the negative version of these words or other comparable words.  Such forward-looking statements are subject to various risks and uncertainties including, among other things: our ability to achieve or sustain profitability in the future; our ability to demonstrate to spine surgeons the merits of our products; pricing pressures and our ability to compete effectively generally; collaboration and consolidation in hospital purchasing; inadequate coverage and reimbursement for our products from third-party payors; lack of long-term clinical data supporting the safety and efficacy of our products; dependence on a limited number of third-party suppliers; our ability to maintain and expand our network of direct sales employees, independent sales agencies and international distributors and their level of sales or distribution activity with respect to our products; proliferation of physician-owned distributorships in our industry; decline in the sale of certain key products; loss of key personnel; our ability to enhance our product offerings through research and development; our ability to manage expected growth; our ability to successfully acquire or invest in new or complementary businesses, products or technologies; our ability to educate surgeons on the safe and appropriate use of our products; costs associated with high levels of inventory; impairment of our goodwill and intangible assets; disruptions in our main facility or information technology systems;  our ability to ship a sufficient number of our products to meet demand; our ability to strengthen our brand; fluctuations in insurance cost and availability; our ability to comply with extensive governmental regulation within the United States and foreign jurisdictions; our ability  to maintain or obtain regulatory approvals and clearances within the United States and foreign jurisdictions; voluntary corrective actions by us or our distribution or other business partners or agency enforcement actions; recalls or serious safety issues with our products; enforcement actions by regulatory agencies for improper marketing or promotion; misuse or off-label use of our products; delays or failures in clinical trials and results of clinical trials; legal restrictions on our procurement, use, processing, manufacturing or distribution of allograft bone tissue; negative publicity concerning methods of tissue recovery and screening of donor tissue; costs and liabilities relating to environmental laws and regulations;  our failure or the failure of our agents to comply with fraud and abuse laws; U.S. legislative or Food and Drug Administration regulatory reforms; adverse effects of medical device tax provisions; potential tax changes in jurisdictions in which we conduct business; our ability to generate significant sales; potential fluctuations in sales volumes and our results of operations over the course of the year; uncertainty in future capital needs and availability of capital to meet our needs; our level of indebtedness and the availability of borrowings under our credit facility; restrictive covenants and the impact of other provisions in the indenture governing our convertible  senior notes and our credit facility;  continuing worldwide economic instability; our ability to protect our intellectual property rights; patent litigation and product liability lawsuits; damages relating to trade secrets or non-competition or non-solicitation agreements; risks associated with operating internationally; fluctuations in foreign currency exchange rates; our ability to comply with the Foreign Corrupt Practices Act and similar laws; increased costs and additional regulations and requirements as a result of being a public company; our ability to implement and maintain effective internal control over financial reporting; potential volatility in our stock due to sales of additional shares by our pre-IPO owners or otherwise; our lack of current plans to pay cash dividends; our ability to take advantage of certain reduced disclosure requirements and exemptions as a result of being an emerging growth company; potential dilution by the future issuances of additional common stock in connection with our incentive plans, acquisitions or otherwise; anti-takeover provisions in our organizational documents and our ability to issue preferred stock without shareholder approval; potential limits on our ability to use our net operating loss carryforwards; and other risks and uncertainties, including those described under the section entitled “Risk Factors” in our most recent Annual Report on Form 10-K filed with the SEC, as such factors may be updated from time to time in our periodic filings with the SEC, which are accessible on the SEC’s website at www.sec.gov.  Accordingly, there are or will be important factors that could cause actual outcomes or results to differ materially from those indicated in these statements.  These factors should not be construed as exhaustive and should be read in conjunction with the other cautionary statements that are included in this release and our filings with the SEC.

We operate in a very competitive and challenging environment.  New risks and uncertainties emerge from time to time, and it is not possible for us to predict all risks and uncertainties that could have an impact on the forward-looking statements contained in this release.  We cannot assure you that the results, events and circumstances reflected in the forward-looking statements will be achieved or occur, and actual results, events or circumstances could differ materially from those described in the forward-looking statements.

The forward-looking statements made in this press release relate only to events as of the date on which the statements are made.  We undertake no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as required by law.  We may not actually achieve the plans, intentions or expectations disclosed in our forward-looking statements and you should not place undue reliance on our forward-looking statements. Unless specifically stated otherwise, our forward-looking statements do not reflect the potential impact of any future acquisitions, mergers, dispositions, joint ventures, investments or other strategic transactions we may make.

Media Contact: Zeno Group on behalf of K2M Group Holdings, Inc. Christian Emering, 212-299-8985 Christian.Emering@ZenoGroup.com  Investor Contact: Westwicke Partners on behalf of K2M Group Holdings, Inc. Mike Piccinino, CFA, 443-213-0500 K2M@westwicke.com

New Guideline Aims to Reduce Infections in Total Hip and Knee Replacement Patients

American College of Rheumatology – For Immediate Release, June 16, 2017

ATLANTA – According to a new guideline released by the American College of Rheumatology (ACR) and American Association of Hip and Knee Surgeons (AAHKS), the risk of joint infection resulting from total hip and knee replacements can be reduced with careful management of anti-rheumatic medications during the perioperative process. The guideline represents the first time rheumatologists and orthopaedic surgeons have collaborated to develop recommendations.

“Periprosthetic joint infection remains one of the most common reasons for failure of hip and knee replacement,” said Bryan D. Springer, MD, an orthopedic surgeon at the OrthoCarolina Hip and Knee Center in Charlotte, N.C., and AAHKS Education Council Chair, who served as a co-principal investigator for the guideline project. “Because periprosthetic joint infections are associated with such high morbidity and mortality, we felt there was a dire need for perioperative management recommendations that could be subscribed to by both disciplines in order to provide arthritis patients with better outcomes.”

The guideline includes eight recommendations regarding when to continue, withhold and re-start medications commonly used to treat inflammatory rheumatic diseases (e.g., rheumatoid arthritis, spondyloarthritis and systemic lupus erythematosus), as well as the optimal perioperative dosing of glucocorticoids. Key recommendations for reducing the risk of infection include:

  • Discontinuing biologic therapy prior to surgery in patients with inflammatory arthritis.
  • Withholding tofacitinib for at least seven days prior to surgery in rheumatoid arthritis, spondyloarthritis and juvenile idiopathic arthritis patients.
  • Withholding rituximab and belimumab prior to surgery in all systemic lupus erythematosus patients undergoing arthroplasty.

In addition to rheumatology and orthopedic experts, a patient panel was incorporated to ensure the guidelines adequately represented patients’ concerns and preferences.

 

READ THE REST HERE

ConforMIS Announces FDA 510(k) Clearance for iTotal Hip System

BILLERICA, Mass., June 20, 2017 (GLOBE NEWSWIRE) — ConforMIS, Inc. (NASDAQ:CFMS), a medical technology company that offers knee replacement implants customized to fit each patient’s unique anatomy, today announced it has received FDA 510(k) clearance of the Company’s primary iTotal Hip replacement system.

“Having treated over 50,000 patients with customized knee replacement implants, ConforMIS brings over a decade of experience in patient-specific technology to the hip replacement market,” said Mark Augusti, Chief Executive Officer and President of ConforMIS.  “FDA clearance of iTotal Hip demonstrates the ability to apply our proprietary iFit® image-to-implant technology to other joints.  There has been a trend towards personalized healthcare and we believe patients expect and deserve personalized treatment.”

The ConforMIS iTotal Hip system features proprietary iFit technology similar to that used to design, manufacture and deliver customized knee implants.  The system utilizes ConforMIS’s patient-specific technology, single-use 3D printed instruments and just-in-time delivery model to create a system that requires limited reusable instruments.

“Standard hip replacement surgery can be challenging, presenting risks of dislocation, discrepancies in leg length and limited reproducibility,” said Scott Ball, MD, Department of Orthopaedic Surgery, University of California, San Diego and a member of the iTotal Hip design team.  “With the ability to achieve a better match to a patient’s own anatomy, the iTotal Hip system aims to address these shortcomings and improve patient outcomes.”

“We expect to leverage synergies with sales representatives, surgeons and hospitals upon limited launch, which is anticipated for 2019,” added Augusti.  “We are excited about the opportunity iTotal Hip represents in expanding our product portfolio to address a broader orthopedic market with our proprietary technology.”

In the United States, approximately 400,000 hip replacements were performed in 2016.  The global hip joint reconstruction market is projected at over $6B.

 

A photo accompanying this announcement is available at:

http://www.globenewswire.com/NewsRoom/AttachmentNg/a2f06ce1-6e8f-4f5e-b521-0a2f9b95aef4

EOI is Raising the Bar in MIS Fusion Surgeries With its FLXfit™ 3D Expandable Cage

OR AKIVA, Israel, June 19, 2017 /PRNewswire/ —

Expanding Orthopedics Inc. (EOI), a medical device company focused on developing and commercializing innovative expandable devices for spine surgery, is proud to announce that Dr. Claudio Feler of the Cheyenne Regional Medical Group has adopted the FLXfit™ 3D Expandable TLIF Cage as his implant of choice for his MIS TLIF procedures. Dr. Feler noted that “Large bodies of clinical evidence show that lordotic restoration is crucial in addressing sagittal alignment. FLXfit’s™ unique articulating design allows for a very large implant footprint to pass through an MIS cannula and be positioned in the anterior portion of the disc space”.

Dr. Claudio Feler, Cheyenne Regional Medical Group and Associate Professor in the Department of Neurosurgery at the University of Tennessee Medical Center said, “The MIS FLXfit™ Inserter has been specifically designed to go through a narrow access tube and maintain clear line of sight while utilizing a microscope.” He added that “sagittal alignment improves outcomes and negates possible adjacent level disease. Functionally, patients tend to have less back pain postoperatively and less potential slip and falls as their horizontal gaze is corrected.” Dr. Feler concluded “FLXfit™ offers a superior approach for my surgical practice as the dial in lordosis is positioned optimally to help achieve sagittal alignment”.

Ofer Bokobza, CEO of EOI, says that “we are excited with our continued collaboration with Dr. Feler. As an early adopter in minimal invasive spine surgery and pioneer in interventional pain management, he recognizes the value of FLXfit™ for MIS surgery. His valued input has successfully helped us realize the new FLXfit™ MIS System”. Ofer emphasizes that “EOI recognizes the need for continuous innovation and the introduction of novel solutions through collaboration with leading surgeons. We believe that the FLXfit™ MIS system is raising the bar again and will help many surgeons transition to MIS spine surgery”.

About Expanding Orthopedics Inc.

Expanding Orthopedics Inc. is medical device company developing and marketing innovative products designed to address unmet clinical needs for spine care and improve long-term patients’ outcome. The Company is spearheaded by seasoned management team, and is advised by prominent spine surgeons. EOI owns a broad patent portfolio around anatomically fit, expandable devices for enhanced stability through MIS approach.

Contact info:
David Elkaim, VP Marketing and Sales
E-mail: david@xortho.com
Phone: (347) 3219683

SOURCE Expanding Orthopedics Inc.

Next Generation Lumbar Fusion Devices by Meditech Spine Aims to Improve Surgical Outcomes, Receives FDA Clearance

ATLANTA, June 19, 2017 /PRNewswire/ — Spine surgery offers a new lease on life for patients experiencing back pain and discomfort. With an estimated 450,000+ lumbar fusions performed each year in the United States, surgeons are familiar with Meditech Spine’s Talos® Lumbar Peek devices as essential components in the procedures they perform. And now Meditech offers surgeons the next generation of their already successful devices, the Talos® Lumbar (HA) Peek IBF that has received US Federal Drug Administration (FDA) 510(k) clearance to be marketed.

Surgeons treating patients with Degenerative Disc Disease (DDD), defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies, consider a lumbar decompression and fusion to help relieve symptoms in the spine. Meditech’s Talos® Lumbar (HA) Peek IBF device is an intervertebral body device intended for use in skeletally mature patients with DDD of the lumbar spine with up to Grade 1 spondylolisthesis at one or two contiguous levels from L2-S1. These devices are intended to be used with autograft and/or allograft comprised of cancellous and/or corticocancellous bone graft.

The Talos® Peek Lumbar IBF devices have been adopted and utilized throughout the US market since 2010. With this most recent FDA approval, Meditech will now market the Talos® lumbar interbodies with Invibio Biomaterial Solutions, PEEK-OPTIMA® HA Enhanced material.

PEEK-OPTIMA® HA Enhanced is a novel material for these interbody cages, contributing to the fusion process as it is strong, versatile and based on PEEK-OPTIMA® polymer compounded with hydroxyapatite (HA), a well-known osteoconductive material for enhancing bone apposition. This component is not a secondary surface coating or added texture but is completely integrated throughout the polymer and, consequently, throughout the implant and all surfaces. Since Meditech’s Talos®-C (HA) Cervical IBF clearance in 2015, Meditech and surgeons have observed similar results that mimic a preclinical ovine study that demonstrated better ongrowth and improved fusion when compared to Peek alone1 .

“We took a ‘wait and see’ approach with our introduction of HA Peek in our cervical implants in 2015,” says Eric Flickinger, co-founder of Meditech Spine. “With nearly two years of data, we saw enough clinical evidence and heard enough positive surgeon feedback to convince us to move our lumbar portfolio to this new technology. Bone ongrowth, and better and faster fusion outcomes are what surgeons look for in their patient follow up. This is exactly what we have seen, similar to the preclinical ovine study, with our cervical IBFs with PEEK-OPTIMA® HA Enhanced material.”

The Talos® HA Peek Lumbar System is a family of interbody devices that allows surgeons to choose their preferred method of approach for each patient whether it be a PLIF, TLIF, TPLIF, ALIF or LLIF. Meditech will introduce the six different lumbar IBF footprints of Talos®-P (HA), Talos®-P WB (HA), Talos®-T (HA), Talos®-TL (HA), Talos®-A (HA) and Talos®-L (HA) later this year. With this release, Meditech has added more footprints as well as hyperlordotic and asymmetric sizes to meet surgeons’ needs for their patients. The devices are designed with large graft windows to allow packing of autograft or allograft and come with disc preparation instruments to help facilitate and streamline the procedure. All the Talos® IBF implants will continue to be supplied in sterile packaging to aid in traceability and help reduce possible infection.

1.

Walsh WR, Pelletier MH, Bertollo N, Christou C, Tan C. Does PEEK/HA Enhance Bone Formation Compared With PEEK in a Sheep Cervical Fusion Model? Clin Orthop Relat Res. 2016; DOI 10.1007/s11999-016-4994-x

ABOUT MEDITECH SPINE

Meditech Spine, LLC, is a spinal implant company that partners with leaders in the industry to design, develop, and distribute implant devices that make a positive difference in the market. Meditech’s pursuit of novel and innovative technologies drives its design and development team. As Meditech builds on its IP platform, it seeks strategic partnerships and applications to provide surgeons and patients with the best available technologies. For more information visit www.meditechspine.com.

Caption & Copyright:
Talos® and Meditech logos are registered trademarks of Meditech Spine, LLC. All rights reserved. PEEK-OPTIMA® is a registered trademark of Invibio, Ltd. All rights reserved.

Meditech Spine, LLC
1447 Peachtree Street, Suite 440
Atlanta, GA 30309
Phone: 678-974-5287
Email: support@meditechspine.com

 

SOURCE Meditech Spine, LLC

Related Links

http://www.meditechspine.com

Stryker announces definitive agreement to acquire NOVADAQ Technologies Inc.

By GlobeNewswire

Kalamazoo, Michigan – June 19, 2017- Stryker Corporation (NYSE:SYK) announced today a definitive agreement to acquire NOVADAQ Technologies Inc. (NASDAQ:NVDQ; TSX:NDQ) for US$11.75 per share, or US$701 million with a net purchase price of US$654 million, reflecting net cash of approximately US$47 million. NOVADAQ is a leading developer of fluorescence imaging technology that provides surgeons with visualization of blood flow in vessels, and related tissue perfusion in cardiac, cardiovascular, gastrointestinal, plastic, microsurgical, and reconstructive procedures.  NOVADAQ was founded in 2000 and is headquartered in Mississauga, Canada.

“This acquisition aligns with Stryker’s focus on enabling our customers to see and do more by enhancing cross-specialty surgical visualization,” stated Timothy J. Scannell, Group President, MedSurg and NeuroTechnology. “NOVADAQ’S unique innovative technology complements Stryker’s advanced imaging portfolio and expands our product offerings into open and plastic reconstructive surgery. NOVADAQ’S innovative technology can reduce post-procedure complication rates and the cost of care for a broad variety of surgical treatments.”

“This transformative transaction recognizes the exceptional value we have built at NOVADAQ. Moreover, we believe it creates a strong opportunity for NOVADAQ, its customers, partners, shareholders, and employees,” said Rick Mangat, President and Chief Executive Officer of NOVADAQ. “I am proud of the impact our SPY and PINPOINT technology has made throughout the world in breast reconstruction and colorectal surgery, as well as other minimally invasive applications, and look forward to the additional progress we can make as part of Stryker’s organization.”

The transaction is structured as an arrangement under the Canada Business Corporations Act, subject to customary closing conditions, including approval by NOVADAQ’S shareholders and the Ontario Superior Court of Justice, the expiration or termination of the Hart-Scott-Rodino Antitrust Improvements Act waiting period and clearance under the Competition Act (Canada).  The transaction is expected to close at the end of the third quarter and is expected to be dilutive to Stryker’s 2017 adjusted net earnings per diluted share by $0.03 – $0.05. There is no change to Stryker’s 2017 estimated adjusted net earnings per diluted share, which is in the range of $6.35 – $6.45. For 2018, this transaction is expected to be neutral to Stryker’s earnings and accretive thereafter.

Covington & Burling LLP and Osler, Hoskin & Harcourt LLP are serving as outside legal counsel for Stryker in connection with this transaction.

Forward-looking statements

This press release contains information that includes or is based on forward-looking statements within the meaning of the federal securities law that are subject to various risks and uncertainties that could cause our actual results to differ materially from those expressed or implied in such statements. Such factors include, but are not limited to: weakening of economic conditions that could adversely affect the level of demand for our products; pricing pressures generally, including cost-containment measures that could adversely affect the price of or demand for our products; changes in foreign exchange markets; legislative and regulatory actions; unanticipated issues arising in connection with clinical studies and otherwise that affect U.S. Food and Drug Administration approval of new products; potential supply disruptions; changes in reimbursement levels from third-party payors; a significant increase in product liability claims; the ultimate total cost with respect to the Rejuvenate and ABG II matter; the impact of investigative and legal proceedings and compliance risks; resolution of tax audits; the impact of the federal legislation to reform the United States healthcare system; changes in financial markets; changes in the competitive environment; our ability to integrate acquisitions, including the acquisition of NOVADAQ; and our ability to realize anticipated cost savings. Additional information concerning these and other factors is contained in our filings with the U.S. Securities and Exchange Commission, including our Annual Report on Form 10-K and Quarterly Reports on Form 10-Q.

Stryker is one of the world’s leading medical technology companies and, together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. Stryker is active in over 100 countries around the world.  Please contact us for more information at www.stryker.com.

Contacts

For investor inquiries please contact:

Katherine A. Owen, Stryker Corporation, 269-385-2600 or katherine.owen@stryker.com

For media inquiries please contact:

Yin Becker, Stryker Corporation, 269-385-2600 or yin.becker@stryker.com

This announcement is distributed by Nasdaq Corporate Solutions on behalf of Nasdaq Corporate Solutions clients.

The issuer of this announcement warrants that they are solely responsible for the content, accuracy and originality of the information contained therein.

Source: Stryker Corporation via Globenewswire