Medicrea to Participate in the Canaccord Genuity Musculoskeletal Conference and Present Clinical Results at AAOS 2018

March 05, 2018

LYON, France & NEW YORK–(BUSINESS WIRE)–The Medicrea Group (Euronext Growth Paris: FR0004178572 – ALMED), pioneering the convergence of healthcare IT and next-generation, outcome-centered spinal device design and manufacturing with UNiD ASI™ (Adaptive Spine Intelligence) technology, announced today that the Company will present at the Canaccord Genuity Musculoskeletal Conference on Tuesday, March 6, 2018 at 11:30 a.m. CT (6:30 p.m. GMT+1) at the Sheraton New Orleans Hotel in New Orleans, LA.

Clinical results on the Company’s patient-specific UNiD™ Rod will be presented by Dr. Andrew King at the Annual Meeting of the American Academy of Orthopaedic Surgeons (AAOS). The podium, entitled “Radiographic Comparison of Patient-Specific and Manually Contoured Conventional Rods in Adolescent Idiopathic Scoliosis Surgery”, will take place in the session beginning at 11:00 a.m. CT (6:00 p.m. GMT+1) held in Room 345 of the Morial Convention Center on Friday, March 9th.

About Medicrea (www.medicrea.com)

Through the lens of predictive medicine, Medicrea leads the design, integrated manufacture, and distribution of 30+ FDA approved spinal implant technologies that have been utilized in over 150,000 spinal surgeries to date. By leveraging its proprietary software analysis tools with big data and machine learning technologies and supported by an expansive collection of clinical and scientific data, Medicrea is well-placed to streamline the efficiency of spinal care, reduce procedural complications and limit time spent in the operating room.

Operating in a $10 billion marketplace, Medicrea is a Small and Medium sized Enterprise (SME) with 175 employees worldwide, which includes 50 who are based in the U.S. The Company has an ultra-modern manufacturing facility in Lyon, France housing the development and production of 3D-printed titanium patient-specific implants.

For further information, please visit: Medicrea.com.

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

Medicrea is listed on
EURONEXT Growth Paris
ISIN: FR 0004178572
Ticker: ALMED
LEI: 969500BR1CPTYMTJBA37

Contacts

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

Spineology Receives a Notice of Allowance for a New US Patent on its Duo™ Lumbar Interbody Fusion Implant

March 05, 2018

ST. PAUL, Minn.–(BUSINESS WIRE)–Spineology Inc., an innovator in anatomy-conserving spine surgery, is excited to announce it has received a Notice of Allowance from the United States Patent and Trademark Office (USPTO) for patent application No. 15/476,911, “Mesh Spacer Hybrid.” The allowed claims include three independent device claims covering Spineology’s Duo implant, a novel proprietary intervertebral implant that includes PEEK intervertebral spacer elements and an expandable mesh graft containment element. Spineology expects the patent to be issued within the next several weeks.

“We always strive to attain protection for strategic intellectual property,” said John Booth, Chief Executive Officer of Spineology. “This Notice of Allowance is an important extension to our IP Portfolio.”

The Duo System implant is the first to combine PEEK, titanium and graft containment mesh elements. This design dramatically reduces the access required to implant a device compared to traditional lateral systems. By significantly minimizing the nerve and soft tissue retraction typically required in these surgeries, the company believes the Duo System will reduce the post-operative thigh pain and other complications commonly associated with the lateral approach. In addition to reducing the exposure required for placement, the Duo implant, once filled, creates a large, load-sharing, endplate-conforming graft pack that expands up to 30mm in width to help maintain spinal correction and support fusion.

About Spineology Inc.
Spineology Inc. provides innovative, anatomy-conserving spinal technologies for surgeons and their patients. Spineology surgical techniques conserve spinal bone, ligament and muscle tissue. Spineology is committed to increasing procedural efficiency, reducing surgical morbidity and accelerating patient recovery. Learn more at spineology.com.

Contacts

Spineology Inc.
John Booth, 651-256-8511
jbooth@spineology.com
or
Risdall
Dave Folkens, 651-286-6713
dave@risdall.com

Laser Spine Institute Announces Thomas Linton as Chief Patient Empowerment Officer

February 28, 2018 (TAMPA, Fla.) – Laser Spine Institute, the leader in minimally invasive spine surgery, today announced the appointment of Thomas Linton as its first-ever Chief Patient Empowerment Officer. Linton previously served as Vice President of Customer Experience at Assurant, a Fortune 500 insurance company.

“We look forward to leveraging Thomas’ expertise to further facilitate the delivery of exemplary experiences for our patients during every step of their care journey,” said Roger Cary, President and Chief Executive Officer, Laser Spine Institute. “Creating this position and adding someone with Thomas’ track record is a testament to our commitment to patient-centered care.”

As Chief Patient Empowerment Officer, Linton will have oversight of the organization’s patient-facing teammates who serve as the first touch in the patient experience, those who are the patient’s main contact throughout their journey and liaisons with physicians in local markets. Linton will also help identify patients’ interactions, which are critical moments of truth, to improve their overall experience.

Linton has more than 20 years of experience in marketing, sales and customer experience, with a focus on delivering customer-centered solutions. Prior to joining Laser Spine Institute, Linton also held leadership positions at AT&T, Bank of America and General Electric. Linton’s years of experience have made him known for his effectiveness in driving growth, improving efficiencies and finding customer solutions.

“I’m thrilled to be joining a purpose-driven organization and to play a part in continuing Laser Spine Institute’s mission to provide exceptional patient experiences and care,” Linton said. “We are known as the leader in minimally invasive spine surgery for a reason, and the impact our teammates and innovative medicine plays on our patients’ lives was instrumental in my decision to join the organization.”

Linton received his Master of Business Administration in marketing and strategic planning from the Wharton School at University of Pennsylvania. He also holds a Bachelor of Science in electrical engineering and a Master of Engineering from the University of Louisville. He serves on the Board of Directors for the George M. Hughes Foundation, which provides college scholarships to deserving high school seniors.

For more information, visit http://news.laserspineinstitute.com/.

Media Contact: Maura Devetski, Edelman
Phone: 404-832-6788
Email: maura.devetski@edelman.com

About Laser Spine Institute
Headquartered in Tampa, Florida, Laser Spine Institute currently operates seven regional surgery centers across the country, in Tampa, Florida; Scottsdale, Arizona; Philadelphia; Oklahoma City; Cleveland, St. Louis and Cincinnati. Laser Spine Institute has helped more than 75,000 patients find relief from debilitating neck and back pain caused by spinal stenosis, degenerative disc disease, pinched nerves, bone spurs, bulging/herniated discs, sciatica and other chronic conditions. Patients often refer a friend or family member to have surgery at Laser Spine Institute; we have a patient recommendation score of 97 out of 100. Additionally, Laser Spine Institute has been repeatedly recognized for outstanding patient satisfaction and reports an enterprise patient satisfaction score of more than 96.

Laser Spine Institute has been named a top employer by Modern Healthcare, Tampa Bay Times, Tampa Bay Business Journal, Philly.com and okc.BIZ and a Most Admired Company by BestCompaniesAZ. Opening in Tampa in 2005 with one operating room and nine employees, Laser Spine Institute now has nearly 1,000 corporate and health care professionals across the country.

Simplify Medical Announces 50th U.S. Patent for Innovative Cervical Disc Replacement Portfolio

February 27, 2018

SUNNYVALE, Calif.–(BUSINESS WIRE)–Simplify Medical Pty Ltd, maker of the Simplify® cervical artificial disc, today announced receipt of the company’s 50th U.S. patent for its innovative cervical motion preservation intellectual property (IP) portfolio. The Simplify Disc is designed to minimize patient risk associated with radiation, optimize long-term durability, simplify implantation and increase access to cervical disc replacement for patients with smaller anatomies.

The company’s 50th patent, U.S. Patent No. 9,883,945, is entitled “Artificial Intervertebral Disc with Lower Height” and relates to the unique low-profile and more anatomically-shaped disc design. Other recent patents include U.S. Patent No. 9,839,532, covering Simplify Medical’s proprietary methods for inserting intervertebral discs in a less traumatic manner, and U.S. Patent No. 9,839,525, relating to implanting intervertebral discs with a movable core and a protrusion for holding the core captive between endplates.

“Simplify Medical is committed to innovation that improves clinical outcomes for patients with degenerative disc disease,” said Simplify Medical CEO David Hovda. “We believe Simplify Medical has the largest and most impactful IP portfolio in the spine motion preservation space, and we continue to invest in technology to further optimize patient outcomes and surgical ease of use.”

The Simplify Disc is anatomically designed with low height implant options, as low as four millimeters, to treat a broad range of patients, including patients with smaller cervical disc spaces.

Composed of primarily non-metal materials (PEEK-on-ceramic), the Simplify Disc is designed to be viewed on magnetic resonance imaging (MRI) in order to minimize post-operative patient exposure to radiation from computed tomography (CT) scans currently necessary to view metal discs. While MRI is widely used pre-operatively for surgical planning, spine surgeons often switch to CT scans post-operatively in order to accommodate metal components, which can make it difficult to view the devices, as well as the facets and adjacent disc levels. However, CT scans have been shown to expose patients to ionizing radiation that equates to 400 to 550 chest X-rays per scan. The device is considered MRI-conditional, posing no known hazard in an MRI environment within prescribed conditions of use.

The Simplify Disc is being studied in two U.S. pivotal trials. The one-level, prospective trial comparing Simplify Disc with cervical fusion surgery at one level between C3 to C7 has completed enrollment. Use of the Simplify Disc in two levels of the spine is being studied in a second IDE trial in the U.S., which is approximately 40 percent enrolled, and enrollment is expected to be completed by the end of 2018. The two-level, prospective pivotal trial will encompass up to 200 patients at up to 18 centers, comparing cervical implantation of the device in two contiguous discs from C3 to C7 with two-level cervical fusion surgery. For information about eligibility or enrollment in the two-level pivotal trial, please visit http://www.simplifytrial.com/.

The Simplify Disc has received the CE Mark and is commercially available in select European markets. Early clinical data has shown substantial improvement in patient pain scores and functional improvement after treatment.

ABOUT SIMPLIFY MEDICAL

Simplify Medical is focused on cervical spinal disc arthroplasty, using innovative, MRI-friendly materials designed to decrease the need for ionizing radiation and enhance patient options. Simplify Medical is located in Sunnyvale, California. To learn more, visit http://www.simplifymedical.com/.

Caution: The Simplify Disc is an investigational device in the United States and is limited by law to investigational use.

Contacts

Chronic Communications Inc.
Michelle McAdam, (949) 545-6654
michelle@chronic-comm.com

K2M and International Spine Study Group Foundation Collaborate to Advance Data Management Using BACS®

LEESBURG, Va., Feb. 26, 2018 (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 licensure of its BACS® Data Management tool to the International Spine Study Group Foundation (ISSGF) for collecting spine patient data, including patient reported outcome measures (PROMs), as part of the ISSGF’s globally recognized research studies.

BACS Data Management is K2M’s cloud-based data collection and operative reporting system to track outcome metrics on surgical and non-surgical spine patients. These patients use tablets to report symptoms throughout their full episode of care, and surgeons can seamlessly input and analyze diagnostic data, surgical information, and radiographic imagery to better determine treatment specific to each patient.

“On behalf of the ISSGF, I am pleased that K2M’s BACS Data Management system will support our vision of translating clinical research into care of patients with many different spinal pathologies,” said Shay Bess, MD, founder and president of the ISSGF. “Effectively collecting and assessing clinical data is an important aspect for not only tracking patient outcomes, but also for identifying the most effective treatment options. K2M is an innovation leader in spine care and we are excited to partner with them in this effort.”

The ISSGF is a group of approximately 30 surgeons from around the world dedicated to the advancement of treatment for adults with spinal deformity. Members of the ISSGF practice at sites across the United States, Canada, and Japan, combining efforts to produce meaningful, cutting-edge research with the goal of advancing the evaluation, treatment, and outcomes for adult spinal deformity. The members constantly analyze the clinical applications of their research, working to put their findings into the context of improved patient care and outcomes. The ISSGF has presented more than 900 abstracts and published more than 200 manuscripts since the foundation was formed in 2010.

“K2M and the International Spine Study Group Foundation share a common belief—that advancements in spinal surgery increasingly come from technologies that let surgeons put the entire patient journey at the heart of treatment,” said K2M Chairman, President, and CEO Eric Major. “K2M continues to offer solutions to address the ever-changing healthcare landscape; K2M’s BACS Data Management allows the ISSGF to effectively and efficiently collect patient data as they develop predictive analytics models to help physicians tailor treatment approaches specific to each patient’s pathology.”

BACS Data Management is part of K2M’s comprehensive Balance ACS® (BACS) platform, which applies three-dimensional solutions across the entire clinical care continuum to help drive quality outcomes in spine patients. BACS provides solutions to help surgeons achieve 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 K2M, visit www.K2M.com. For more information on 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 FacebookTwitterInstagramLinkedIn 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 and retain their use of our products; pricing pressures and our ability to compete effectively generally in our industry; collaboration and consolidation in hospital purchasing; inadequate coverage and reimbursement for our products from third-party payers; 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 the 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 to our corporate headquarters and operations facilities or critical information technology systems, distributors or surgeon users; 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; our ability to implement and maintain effective internal control over financial reporting; potential volatility in our stock price; our lack of current plans to pay cash dividends; increased costs and additional regulations and requirements as a result of no longer qualifying as an emerging growth company as of December 31, 2017; 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 and our Quarterly Report filed with the SEC on November 1, 2017, 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

Ortho Sales Partners Announces Two Executive Additions and the Formation of Two Divisions (Orthopedics and Spine)

Ortho Sales Partners, the global leader in commercialization services for the orthopedic industry, is pleased to announce key additions allowing the formation of two separate divisions. This strategic move further demonstrates Ortho Sales Partners commitment to offer the industries most talented and experienced consultants to its clients. In advance of their presence at the American Academy of Orthopedic Surgeons annual conference (Booth 5713), Ortho Sales Partners announces the formation of two distinct divisions. One for Orthopedics and the other for Spine. Hired to lead the Orthopedic division are Jeff Chandler and Dan Darges.

Jeff Chandler, has been appointed General Manager of Orthopedics. Mr. Chandler has a rich history in commercializing products in Total Joint Reconstruction, Trauma and Sports Medicine. A key entrepreneurial career highlight featured Mr. Chandler as Founder & CEO/President of a venture capital backed medical device firm (Aquarius Medical), led the Company for six years incepting two core technologies (fluid management pump; core body thermoregulation from Stanford University OTL), and through product inventions (IP), funding, research, development, regulatory, manufacturing, commercialization, and into a successful exit.

About his joining Ortho Sales Partners, Jeff Chandler said: “I’m excited to bring a novel and cost-effective commercialization model to startup and emerging growth companies, or launching disruptive technologies for established medical device firms. In the entrepreneurial spirit of preserving expensive cash, OSP provides an attractive staged-based vehicle to deploy a multi-disciplined and highly networked senior level team in comparison to being confined by traditionally limited FTE hiring.”

Dan Darges, Vice President of Orthopedics, career started in 1997 with Smith & Nephew as a Ortho Recon/Trauma rep, Mr. Darges’ successes and reputation led him to accept an offer as a Regional Sales Director for a top Arthrex Distributorship in 2002.  Working for a Distributor allowed Mr. Darges to grow skills as a leader and manager for both Arthrex and Wright Medical product lines in Multiple States.  In 2007, Mr. Darges founded Bio-Surg Solutions, Inc., a Distributorship for Wright Medical.  After many successful years as one of the highest growth distributorships in the country, Mr. Darges sold his Distributorship to Wright Medical in 2012 and became a Senior Director of Sales for Wright Medical’s Foot and Ankle/Biologics products.

“I am really excited to be part of the Ortho Sales Partners team” said Darges. “I feel this role allows me to use my skill sets in multiple facets for multiple companies within the orthopedic industry.  I have enjoyed my time thus far as a consultant and look forward to taking on more responsibility for our clients as the Vice President of Orthopedics.”

For the spine division, Ortho Sales Partners has promoted Matt Stuttle to the position of General Manager. Mr. Stuttle has been in the medical industry for over 18 years. He began his career in spine in 2003 has held executive management positions at Kyphon (acquired by Medtronic in 2008 for $4.3B), Paradigm Spine, SpineWave and most recently Spineart.

“I feel strongly that Ortho Sales Partners is well positioned to facilitate guidance, structure, growth and scale to medical companies worldwide. Our strengths lie in our team; A world class organization of experienced executives across a broad spectrum of specialties, all designed to mitigate risk and speed execution. I’ve had the pleasure of knowing and working closely with Kevin over the last 15 years. His leadership and vast experience lends itself well to the core focus of Ortho Sales Partners; Creating immense value for our clients and their respective shareholders.”

As General Manager’s Jeff and Matt will report in to the CEO, Kevin McGann.

“We welcome Jeff and Dan to Ortho Sales Partners. As we continue to grow our business, it is important we structure and scale the organization that allows for the continued focus on our clients and positive outcomes. Having Matt and Jeff lead our Spine and Orthopedic Divisions will allow us to stay focused while utilizing their experience and leadership skills.”

About Ortho Sales Partners

Ortho Sales Partners has created a unique platform to help companies in any stage commercialize their products in a very efficient way. We have worked closely with many organizations and produced results that have profoundly impacted each client’s business.

Our services are geared to meet you where you are today and help your business grow by utilizing proven industry executives that bring you an objective analysis and recommendations going forward. Our market knowledge is based on current trends and competitive analysis from industry stalwarts from some of the highest growth companies.

Ortho Sales Partners’ headquarters are in Scottsdale, Arizona but we have several offices across the US. (http://www.orthosalespartners.com).

Centinel Spine and Performance Tech Announce Plan for a Season of Success

NEW YORK, Feb. 22, 2018 /PRNewswire/ — Centinel Spine, LLC is pleased to announce that it has extended an endorsement agreement with Performance Tech Motorsports for the entirety of the 2018 IMSA WeatherTech SportsCar Championship season. Centinel Spine first joined the Performance Tech family in January for the Rolex 24 At Daytona. This partnership will support the creation of a platform to educate the public on spinal disease and options that allow individuals to continue to function at a high level.

Centinel Spine, the pioneer of the No-Profile®, Integrated Interbody™ has a 30 year global clinical history of success behind these devices for treatment of degenerative disc disease. The company recently announced the acquisition of the worldwide assets of the prodisc® Total Disc Replacement portfolio. The prodisc line of products represents the most extensive total disc replacement (TDR) portfolio in the world with the longest history of use. The acquisition is the next step in the evolution of Centinel Spine executing on its mission to become the worldwide leading company addressing spinal disease through anterior access to the spine with the widest breadth and depth of technology platforms.

Performance Tech opens up a new type of athlete and patient population that Centinel Spine Chairman & CEO John Viscogliosi can reach and educate. Performance Tech and Team Principal Brent O’Neill are readily supplying athletes to Centinel Spine for examples of athleticism and the wear of high performance endurance.

“Centinel Spine is really an amazing company,” O’Neill said. “Everything they do to give people life after spinal disease is important. If you’re in a sport long enough or in racing long enough, you’ll have an injury and a lot of times it’s to the spine. This is as important to my drivers as it is my crew guys—you can’t do anything with a bad back. Having them as a sponsor is as much about helping a good cause as it is anything else. John and everyone at Centinel are great people and we’re excited to build something with them.”

Centinel Spine is making it an essential goal for 2018 to educate the public, not just the surgeons using its products. Viscogliosi has aligned the company with Performance Tech, as well as PGA Tour golfers, to help reach the masses. Performance Tech will play a primary role in creating the Centinel Spine platform. Viscogliosi is planning on learning as much from Performance Tech as he is educating.

“We are excited to extend our partnership with Performance Tech and continue to get the word out that Centinel Spine has solutions to address spine disease and to allow individuals get their lives back and function at a high level,” Viscogliosi. “The teamwork and commitment to excellence exhibited by the Performance Tech team at the Rolex 24 At Daytona last month confirmed that this is the right partnership to support our mission to raise awareness that spinal injury or disease does not need to result in a change in lifestyle. We are proud to be part of the Performance Tech family and look forward to working as a team to better educate race fans and the general public.”

Viscogliosi and O’Neill get to work this March for the Mobil 1 Twelve Hours of Sebring Presented by Advance Auto Parts. The race week begins Wednesday, March 14, with the crescendo coming at 10:40 a.m. and p.m. Saturday, March 17. The second installment of the Tequila Patròn North American Endurance Championship will air live on various FOX channels. Viewers can catch the start of the Twelve Hours of Sebring on FOX Sports 1 and the finish on FOX Sports 2.

About Centinel Spine, LLC.

Centinel Spine, LLC. is a privately-held spinal device company leading the development and commercialization of the No- Profile, Integrated Interbody fusion technologies. The company recently acquired the prodisc® Total Disc Replacement portfolio, an extensive cervical and lumbar disc replacement platform with the longest history of global clinical use. For more information on Centinel Spine products and technologies, please visit the Company’s website at www.CentinelSpine.com.

The Company began operations in August 2008, through the merger-acquisition of two pioneering medical device companies: Raymedica LLC and Surgicraft LTD. Today, Centinel Spine still embraces the pioneering culture developed at both originating companies and continues its corporate mission of becoming the leading anterior column reconstruction spine franchise, providing elegantly simple implants and instruments that are tissue-sparing and generate superior clinical outcomes.

Centinel Spine derived its name from the “Sentinel Sign” the radiographic confirmation of a successful fusion anterior to the interbody device.

For more information, please contact:

Varun Gandhi
SVP, Corporate Finance & Strategic Planning Centinel Spine, LLC
900 Airport Road, Suite 3B
West Chester, PA 19380
Phone: 484-887-8871
Email: v.gandhi@centinelspine.com

Wendy F. DiCicco
Chief Operating and Chief Financial Officer Centinel Spine, LLC
900 Airport Road, Suite 3B
West Chester, PA 19380
Phone: 484-887-8837
Email: w.dicicco@centinelspine.com

LBL 444 Rev 1 (02/2018)

SOURCE Centinel Spine

 

Related Links
http://www.centinelspine.com

Astura Medical Announces Initial Cases and Full Commercial Release For BRIDALVEIL OCT Stabilization System

CARLSBAD, CA – February 21, 2018 – Astura Medical, a high growth, innovative spine technology company, announced today the completion of the initial surgeries and full commercial release for its BRIDALVEIL Occipital-Cervico-Thoracic (OCT) System. The first cases were successfully completed at multiple hospitals across the country, including at the University of Colorado Hospital by Dr. David Ou-Yang, Assistant Professor of Orthopedics.

“Our practice addresses a wide range of complex conditions, so I’m always looking for the most advanced technology to meet our surgical demands,” said Dr. Ou-Yang. “Bridalveil OCT has not only met those demands, but it has continued to exceed my expectations. The versatility of the instrumentation, coupled with the breadth of implants offered has enhanced our ability to treat even the most complex cases. It is the most comprehensive and one of the most user friendly posterior cervical systems I’ve used from any company, large or small.”

“We are extremely proud of the feedback and success we’ve seen with Bridalveil OCT since our initial release of the system,” said Joel Gambrell, President and CEO of Astura Medical. “It allows us to continue to expand upon our goal of providing market leading technology to our growing network of surgeon and distributor partners.”

Designed with the most complex and demanding cases in mind, BRIDALVEIL OCT provides a comprehensive offering of screw options (single-lead, dual-lead, high-top, and smooth shank) ranging from 3.5mm to 5.5mm in diameter that are compatible with either a 3.5mm or 4.0mm rod in titanium or cobalt chrome. The system additionally provides an extensive line of connectors, transition rods, and instrumentation options to allow surgeons the ability to seamlessly transition across multiple segments of the spine.

About Astura Medical
Astura Medical was formed in 2014 with the objective of creating a disciplined, multi-phased approach to developing, manufacturing, and distributing medical devices. With surgeon input and feedback at every stage of development, Astura has created an extensive line of devices of the highest quality and sleekest design.

The two essential pillars that contribute to Astura Medical’s success are high quality products and robust distribution channels. These pillars, combined with passion and innovation, are what drive the Astura team to achieve great success with developing devices and entering them into the marketplace.

For more information, please visit www.asturamedical.com or find us on LinkedIn.

Media Contact:
Steve Haayen
Astura Medical
858.472.8825
steve@asturamedical.com

EOS imaging Announces First System Installation within Asklepios Private Hospital Group in Germany

February 21, 2018

PARIS–(BUSINESS WIRE)–Regulatory News:

EOS imaging (Paris:EOSI) (Euronext, FR0011191766 – EOSI – Eligible PEA – PME), the pioneer of 2D/3D imaging and data solutions for orthopedics, today announced the first installation of an EOS® system within the Asklepios Hospital Group, the second largest private hospital network in Germany. The EOS system is available at the Asklepios Paulinen Hospital, enabling 3D full-body imaging at a low-dose of radiation, and reinforcing the hospital’s mission as a “Center of Excellence” for back disorders and treatment. The Asklepios Paulinen Hospital hosted a ceremony to celebrate the installation and introduce the community to the EOS system on February 21, 3:00 – 5:00 pm CET.

The Asklepios Paulinen Hospital is a general hospital with 316 beds located in Wiesbaden, Germany that specializes in state-of-the-art methods for improved patient care. In order to diagnose and treat patients in an interdisciplinary manner, it established several specialized medical centers including spinal surgery and orthopedics. With the installation of the EOS system, the spine and orthopedic team has taken another step towards an integrative “Center of Excellence” for the diagnosis and treatment of back disorders. The new device represents a major advance in diagnostics, the subsequent treatment planning and the treatment control of malpositions and deformities of the musculoskeletal system.

“I am thrilled with the new system, which opens up a whole new range of diagnostic options, including more than 100 3D clinical parameters that provide information on the spine’s angular and axial relationships with unprecedented precision. Particularly for patients with deformities like scoliosis, the Micro Dose option is a clear advantage, allowing us to take pictures with minimal radiation while maintaining excellent image quality,” commented Professor Dr. Thomas Niemeyer, Head of the Spine Surgery Department.

“We are pleased to expand our presence in Germany with this installation,” commented Marie Meynadier, Chief Executive Officer of EOS imaging. “The Asklepios Hospital Group is committed to advancing the orthopedic standard of care, as evidenced by building a Center of Excellence for the diagnosis and treatment of back disorders at the Asklepios Paulinen Hospital. We look forward to our technology contributing to this commitment.”

About EOS imaging

EOS imaging designs, develops, and markets EOS®, an innovative medical imaging system dedicated to osteoarticular pathologies and orthopaedics, as well as associated solutions. The Company is authorized to market in 51 countries, including the United States (FDA), Japan and the European Union (EC). The Group posted 2017 sales of €37.1 million and employs 152 people at December 2017. The Group is based in Paris and has five subsidiaries in Besançon (France), Cambridge (Massachusetts), Montreal (Canada), Frankfurt (Germany) and Singapore.

EOS imaging has been selected to integrate the EnterNext © PEA – PME 150 index, composed of 150 French, listed companies on the Euronext markets in Paris.

EOS imaging is listed on Compartment C of Euronext Paris
ISIN: FR0011191766 – Ticker: EOSI

Contacts

EOS imaging
Pierre Schwich, +33 (0)1 55 25 61 24
CFO
investors@eos-imaging.com
or
The Ruth Group (US)
Press relations
Joanna Zimmerman, 646-536-7006
jzimmerman@theruthgroup.com

Spine Wave Launches Proficient® Posterior Cervical Spine System Implants for Complex Posterior Cervical-Thoracic Procedures

SHELTON, Conn., Feb. 21, 2018 (GLOBE NEWSWIRE) — Spine Wave is increasing the Proficient®Posterior Cervical Spine System’s product offering to further serve the posterior cervical spine market.  The system is gaining rapid adoption by spine surgeons, primarily due to its patented tri-lobe polyaxial screw design which offers a best in class 120 degrees of angulation.  Now, the Proficient® Posterior Cervical Spine System is expanded to include a range of new implants that make the system even more versatile for complex posterior cervical-thoracic procedures.

The Proficient® Posterior Cervical Spine System is now offered with a unique translation screw that provides medial-to-lateral translation to facilitate improved rod placement in posterior cervical-thoracic fixation procedures.  Other new Proficient® Posterior Cervical Spine System implants include screw-to-rod lateral connectors, rod-to-rod connectors, and smooth-shank screws as an alternative for fixation of the uppermost cervical spine levels.  Taken together, these new implants make the Proficient® Posterior Cervical Spine System even more appealing for complex posterior cervical-thoracic procedures.

“The Proficient® Posterior Cervical Spine System is an excellent alternative for spine surgeons treating complex posterior cervical-thoracic pathology,” said Peter G. Passias, M.D., FACS, Associate Professor of Orthopaedic and Neurological Surgery, NYU Health, New York, NY.  “The anatomy of the cervical-thoracic junction can make posterior cervical fixation procedures crossing that junction very challenging.  The Proficient® Posterior Cervical Spine System is versatile by design and these new implants make it even more so.”  “In particular,” Dr. Passias continued, “the system’s new translational screw makes rod placement in these procedures faster and easier in my practice because of the unique medial-to-lateral translation capability that it offers.”

“We have been very pleased with how well the Proficient® System has been received in the marketplace. The 120 degrees of angulation has been the biggest selling point and now the system is even more versatile with the advent of the translational screws,” said Mark LoGuidice, Spine Wave CEO. “Historically, Spine Wave has focused on thoraco-lumbar technologies. The Proficient® System is our first internally developed cervical offering and our engineers and surgeon designers have done a phenomenal job with this system.  In addition, we plan to launch a unique anterior cervical technology in the middle of this year. This important anterior system is currently in a limited market release and based on the early feedback, we have high expectations for this system as well.”

/EIN News/ — About Spine Wave

Spine Wave is a leader in expandable fusion technologies and is committed to continually delivering highly differentiated products to enable more efficient and less invasive solutions for spine surgeons and their patients. In addition to the Proficient® Posterior Cervical Spine System, Spine Wave also offers a broad portfolio of expandable devices marketed under the StaXx®, Velocity® and Leva® brand names.  The expandable technologies can be utilized in posterior, anterior and lateral surgical approaches.  To complement the expandable spacers, Spine Wave offers a comprehensive line of pedicle screws for both minimally invasive and traditional open approaches. Additionally, Spine Wave recently launched the GraftMag® Graft Delivery System which is being very well received because it is designed to make interbody bone grafting procedures faster and easier for surgeons.  The company is expanding rapidly and continues to recruit sales managers and independent distributors to fuel growth.  For more information on Spine Wave and its products, please visit www.spinewave.com.

Contact

Terry Brennan, Chief Financial Officer
tbrennan@spinewave.com
(203) 712-1810

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