GS Medical USA Announces New Product Portfolio and Company Enhancements

IRVINE, Calif., Feb. 20, 2017 /PRNewswire/ — GS Solutions Inc., DBA GS Medical USA (GSM), a global manufacturer and supplier of spinal implants, instrumentation and developer of high-quality surgical solutions, today announced several influential advancements for the organization. Following a strong close to the 2016 fiscal year, GSM is poised and prepared for an impactful, growth-oriented year in 2017.

“2017 begins anew for GS Medical with the regeneration of our ‘Expanding New Horizons’ concept,” remarks James Shin, CEO. “Our leadership team has worked tirelessly to lay the foundation for a unique infrastructure system which will continue to cultivate and foster new and existing relationships among our distributor colleagues, surgeons, industry contacts, and hospital partners.” Shin further mentions that many customers already engaged with GSM are excited about the direction and progression of the company.

GSM is pleased to announce the confirmed and pending launch of several products to their existing FDA 510k approved product portfolio. GSM currently offers products under the GSS™ and AnyPlus® product lines, and soon plans to launch the AnyPlus® Anterior Cervical Interbody Fusion (ACIF) implant and the AnyPlus® Dual-Lead Pedicle Screw System in March of 2017. This is in addition to the AnyPlus® Direct Lateral Interbody Fusion (DLIF) implant, slated for a Q2 2017 launch. “The company’s research and development team continues to focus on the essential needs of surgeon partners and their patients, thus yielding fundamental product design and manufacturing that fits the bill on a multitude of levels,” explains Shin. “The introduction of our comprehensive interbody line into the marketplace provides surgeons the option to select the appropriate implant that corresponds with the clinical indications of each individual patient,” states Chris Estuesta, Operations Manager at GSM.

With increased demand for the GS products, the company is also actively seeking distributor partnership opportunities. “Our sales team and industry partners are the lifeline of our company,” explains Adam Lampart, Director of US Sales. “We are always looking for qualified partners who desire to work with a company that is end-user focused, and delivers solid products with timely customer service.” For more information about distributor partner opportunities, please contact sales@gsmedicalusa.com.

About GS Medical USA
GS Medical features many spinal products spanning lumbar, thoracic and cervical applications. GSM products have been used in thousands of spine surgeries throughout the USA, and hundreds of thousands globally. Staffed with a network of industry leaders, medical sales distributors, accomplished engineers, and collaborating physicians, GSM is at the forefront of high-quality, value-added medical technology with a number of innovative implant solutions in the commercialization pipeline. Corporate headquarters are in Irvine, California and with international offices located in Seoul, Korea.

Media Relations Contact:
Amanda Collins
146989@email4pr.com
Phone: 831.477.1307 x213
FAX: 866.600.9712
6 Wrigley
Irvine, CA 92618

www.gsmedicalusa.com

SOURCE GS Medical USA

Related Links

http://www.gsmedicalusa.com

VEXIM: another major step towards the SpineJack® commercialization in the US

Toulouse, February 21st, 2017 (8:00AM CET)VEXIM (FR0011072602 – ALVXM), a medical device company specializing in the minimally-invasive treatment of vertebral fractures, today announces enrollment completion of its FDA clinical trial.

The VEXIM FDA trial is a European, prospective and randomized multicenter study. It aims to compare safety and efficacy of the SpineJack® vs balloon kyphoplasty on 152 patients with osteoporotic vertebral compression fractures. It is being conducted in 12 centers in Germany, France, Italy, Spain and Switzerland. The study is intended to provide clinical data to support a 510(k) submission in the United States, which is expected to be filed by the end of 2017.

« Vertebral Compression Fractures (VCF) represent a true concern in aging population with more than 1.5 million osteoporotic VCF reported each year globally, » explains Professor David Noriega, one of the study investigators.

« Those fractures are very crippling because patients experience acute and chronic back pain, as well as a progressive deformation of the spine that can lead to additional pathologies. Thanks to its jack mechanism, which is designed to restore vertebra from the inside through a mini invasive surgery, the SpineJack® is intended to provide a quick and efficient way of treating those fractures and to restore spine balance[1]. »

VEXIM’s clinical trial compares improvements in terms of back pain, functional and physical capability, quality of life, device safety, analgesic usage and vertebral height restoration, on patients suffering osteoporotic vertebral compression fractures and treated with the SpineJack® and balloon kyphoplasty. Trial’s success will be defined by showing the SpineJack®‘s non-inferiority to balloon kyphoplasty on a primary endpoint which is a composite measure of pain reduction, maintenance or improvement in function and absence of device related serious adverse event.

As of today, all 152 patients planned have been randomized. Half of them within SpineJack® treatment group, the other half in the balloon kyphoplasty group. The finalization of patient enrollment represents an important milestone in the trial’s schedule. SpineJack® 510(k) file is planned to be submitted to the FDA[2] before the end of year 2017.

« The finalization of our FDA clinical study enrollment is a key milestone on the path to commercialize the SpineJack® in the United States. We keep our target to submit our 510(k) in 2017 that would lead, subject to FDA clearance, to a SpineJack® commercialization in the US during the first half of 2018. This is also a demonstration of VEXIM’s capacity to run a large international trial. In the name of VEXIM, I want to thank warmly all our site investigators and coordinators for their active participation that allowed us to achieve this phase of the trial, » concludes Vincent Gardès, VEXIM’s CEO.

Financial reporting schedule:

2016 Full-Year Results: March 22nd, 2017[3]

 

About VEXIM, the innovative back microsurgery specialist

Based in Balma, near Toulouse (France), VEXIM is a medical device company created in February 2006. The Company has specialized in the creation and marketing of minimally-invasive solutions for treating traumatic spinal pathologies. Benefitting from the financial support of it longstanding shareholder, Truffle Capital[4], and from OSEO public subsidies, VEXIM has designed and developed the SpineJack®, a unique implant capable of repairing a fractured vertebra and restoring the balance of the spinal column. The Company currently has 60 members on its staff. It has its own sales teams in France, Germany, Italy, Spain, Switzerland and the United Kingdom, as well as distributors in Turkey, Argentina, India and in the following countries where the product is currently being registered: Mexico, Brazil, Colombia, Venezuela, Chile, Ecuador and Peru. VEXIM has been listed on NYSE Alternext Paris since May 3rd 2012. For further information, please visit www.vexim.com

SpineJack®, an innovative implant for treating Vertebral Compression Fractures

The SpineJack® is designed to restore a fractured vertebra to its original shape, restore the spinal column’s optimal anatomy and thus remove pain and enable the patient to recover their functional capabilities. Thanks to a specialized range of instruments, inserting the implants into the vertebra is carried out by minimally-invasive surgery, guided by X-ray, in approximately 30 minutes, which is intended to enable the patient to be discharged shortly after surgery. The SpineJack® range consists of 3 titanium implants with 3 different diameters, thus covering 95% of vertebral compression fractures and all patient morphologies.

SpineJack® technology benefits from the support of international scientific experts in the field of spine surgery and worldwide patent protection through to 2029.

 

 

CONTACTS
VEXIM

Vincent Gardès, Directeur Général

José Da Gloria, Directeur Administratif et Financier

investisseur@vexim.com

Tél. : +33 5 61 48 48 38

 

RELATIONS PRESSE

ALIZE RP

Caroline Carmagnol / Wendy Rigal

vexim@alizerp.com

Tél. : +33 1 44 54 36 66

Tél. : +33 6 48 82 18 94

Innovasis is pleased to announce the promotion of Mike English to President

Mike joined the company in 2014 and most recently served as the Executive Vice President.  He brings over 20 years of executive leadership experience in medical device and spine including Johnson & Johnson and NuVasive. Innovasis posted significant growth in 2016 while introducing the Excella-MIS system and the PX HA PLIF cage to the market. They are positioned to launch several new products in 2017 and plan to continue building their executive team.

“I’m honored to have the opportunity to lead this extraordinary team. Our positive cash position and strong revenue growth will allow us to continue investing in innovation and talent, “said English.

Innovasis creates growth and value through product innovation and strategic acquisition.  It continues to expand it medical mission work through the International Ortho Neuro Foundation in South America and other nations in need. Innovasis is a manufacturer of spine and cranial implants based in Salt Lake City, UT.

 

You can learn more at www.innovasis.com

 

VTI Moves Its Headquarters To Upgraded Facility

Vertebral Technologies, Inc. a MIS spinal implant medical device company based in Minneapolis, MN, has successfully moved their facilities from Minnetonka, MN to Minneapolis, MN. Brian Thron Director of Marketing says “the contemporary space compliments the company’s latest rebrand, with its simplistic design and modern color scheme. I’m pleased to call this space VTI’s new home”.

“VTI’s new ISO Class 8 Controlled Environment is fully operational post the certification and validation testing process. In addition, the new facility allows VTI to take advantage of increased efficiency across multiple departments with a new office layout that encourages collaboration to everyday operations. We are looking forward to these operative advantages moving forward as VTI grows in 2017”. says Director of Manufacturing Brian Holmberg.

President & CEO Matt Kyle stated “We are excited to be in our new space. The VTI team did a tremendous job of executing the move without disruption. The new space helps everyone align with our organizational objectives and growth focused culture. The feedback we have received, both internal and external, has been very positive.”

ABOUT VTI – VERTEBRAL TECHNOLOGIES, INC.
VTI – Vertebral Technologies, Inc. is a privately held company based in Minneapolis, MN, USA. VTI is dedicated to the design, development, manufacturing and marketing of medical devices to address painful conditions of the spine through less-invasive surgical approaches. VTI’s products utilize its unique modular-assembly technology to deliver solutions optimized for both surgeons and their patients. VTI sells its InterFuse® modular interbody fusion devices worldwide.

For more information, visit: http://www.vti-spine.com or contact Brian Thron at marketing(at)vti-spine(dot)com or + 1.877.912.5401.

Jamaican doctor pioneers disc replacement procedure

Tuesday, February 14, 2017

A group of doctors has high hopes that an artificial disc, owned exclusively by a Jamaican-born doctor, can be used as a tool to drive medical tourism in Jamaica.

The technology was used for the first time in a four-level disc replacement procedure at the Andrews Memorial Hospital in St Andrew on February 1. The surgical procedure was performed by orthopaedic spinal surgeon Dr Kingsley Chin, who was born in Buff Bay, Portland.

Chin is CEO of KIC Ventures, a venture capital firm focused on the health technology sector and the owner of AxioMed, a health tech company that has developed the technology known as the Freedom Cervical disc. AxioMed was founded to advance the standard of care for patients with degenerative spine conditions and has now successfully developed the artificial disc that most closely mimics the normal disc using viscoelastic polymer technology.

In disc replacement, worn or damaged disc material between the small bones in the spine (vertebrae) is removed and replaced with a synthetic or ‘artificial’ disc. The goal of the procedure is to relieve back pain while maintaining more normal motion than is allowed with some other procedures, such as spinal fusion. The Freedom Cervical disc is said to most closely mimic the natural properties of a healthy human disc and has been proven to withstand the forces and wear of decades of use.

On February 1, Dr Chin operated on a female patient with a prolapsed disc who would’ve been in need of several surgical procedures with sequential disc replacement or a fusion of the discs, which would’ve limited her neck motion.

For the procedure, he worked with his team of University of the West Indies (UWI) and Oxford-trained Rhodes Scholar Dr David Walcott, UWI & Yale-trained neurosurgeon Dr J Geoffrey Liburd, and anesthesiologist Dr Patrick Toppin.

 

READ THE REST HERE

Nanovis announces a Successful Alpha Launch of the FortiCore® PLIF and the 2,000th FortiCore® Interbody Implantation.

Carmel and Columbia City, Ind. (February 16, 2017) – Nanovis, a life sciences company committed to developing implant systems that reduce fixation related complications and infections, today announced the successful alpha launch of its FortiCore® PLIF featuring a deeply porous titanium scaffold interdigitated with a PEEK core, and implantation of the 2,000th FortiCore® implant.

“My patient’s short term response to the FortiCore® PLIF has been positive. I implanted the interbody using a minimally invasive technique with no problems. The shape of the implant is favorable for multiple approach options. I’m encouraged by the deep porosity of the titanium scaffold in contact with the vertebral endplate and the pre-clinical data on this technology,” said Dr. Richard B. Rodgers, Goodman Campbell Brain and Spine, a participant in the alpha launch of the FortiCore® PLIF.

With over 2,000 FortiCore® implants now used in surgery, long term clinical experience with FortiCore’s® deeply porous technologies has been positive. “In the 18 months since I started using FortiCore® my patients have been doing well. Initially, I was interested in trying to improve my patient’s outcomes by using a deeply porous titanium scaffold. I’ve been pleased with the excellent radiologic on growth seen on X-ray at 8-12 weeks and the ease of imaging bone through the PEEK core,” said Dr. Gregory Hoffman, Orthopedics North East, an early adopter of the FortiCore® technology.

FortiCore® TLIF and PLIF implants were designed with deeply porous titanium scaffolds to contact the endplate and a radiolucent, favorable-modulus PEEK core injection molded into the bottom of the scaffold creating a durable construct. The FortiCore® TLIF and PLIF systems are available with MIS or open instrumentation.

“Data comparing the osseointegration strength of the FortiCore® scaffold, PEEK and allograft, to the strength of trabecular host bone published in Spine in October, 2016 was encouraging. One of Nanovis’ long term clinical and scientific goals is to reduce fixation related complications so we are delighted to hear positive reports from our customers about their experiences with FortiCore®,” said Matt Hedrick, CEO, Nanovis.

Nanovis is actively recruiting for both employee Area Business Director positions and independent distributor partners and offers an independent distributor referral reward program. For information or a reprint of the Spine article mentioned, please contact Jeff Shepherd, Vice President of Sales, Nanovis at 1-877-907-NANO.

 

About Nanovis

Nanovis’ mission is to lead our select markets with science-enhanced, life-improving technologies.  The Company’s patented and proprietary regenerative technology platforms provide differentiated surface advantages enabling the potential for existing medical devices to achieve new outcomes. Focused on aggressive, sustainable growth across multiple markets, Nanovis is commercializing science-driven platforms: the deeply porous scaffold currently available with the FortiCore® line of interbody fusion devices; a developmental nanosurface technology; and developmental technology with anti-colonization and anti-microbial capabilities.

 

For more information about Nanovis, FortiCore® or other proprietary Nanovis science-enhanced technologies, please visit www.nanovisinc.com or call 1-877-907-NANO.

Caption: Surface Structure: Nanovis’ FortiCore® TLIF interbody fusion devices.

 

Media Contact:

Matt Hedrick

1-877-907-NANO (6266)

Matt.hedrick@nanovistechnology.com

 

Daniel J. Albright, MD Performs Mobi-C Two-Level Cervical Disc Replacement

RALEIGH, NC, February 15, 2017 — Daniel J. Albright, MD announced that he has performed two-level cervical disc replacement procedures utilizing a novel medical device recently approved by the FDA. The procedure was one of the first of its kind in the Raleigh North Carolina area.

The device, the first and only cervical disc replacement FDA approved for both one and two-level applications was the subject of a rigorous FDA Investigational Device Exemption (IDE) trial. In the study, the two-level cervical disc replacement procedure demonstrated an overall study success rate of 69.7% as compared to traditional cervical fusion results of 37.4%. At 24 months, those who received the two-level cervical disc replacement during the trial phase also returned to work on average three weeks earlier as compared to those patients who were treated with cervical fusion. The disc replacement patients also had lower rates of subsequent surgeries and reduced rates of ongoing degeneration at spinal segments adjacent to the surgery.

“I am very proud to be able to offer my patients this state of the art procedure which is supported by the highest level of medical evidence available for a medical device,” said Dr. Albright, of Raleigh Orthopedics. “And for the first time I am able to offer the significant number of my patients who suffer from two-level cervical disease a superior treatment option to traditional cervical spine fusion.”

 

About Daniel Albright, MD
Daniel J Albright, MD is a board certified orthopedic surgeon, who completed two fellowships in spine surgery and total hip and knee replacements. Dr. Albright joined Raleigh Orthopaedic Clinic in 1994.

Dr. Albright completed his undergraduate degree at Dartmouth College in Hanover, New Hampshire, and attended Louisiana State School of Medicine in New Orleans. He completed his residency in orthopedic surgery at Yale-New Haven Hospital. Following residency, Dr. Albright obtained additional training in Spine Surgery at St. Luke’s Medical in Cleveland, Ohio, and Knee & Hip Replacement and Revision Surgery at Massachusetts General Hospital.


Press release service and press release distribution provided by http://www.24-7pressrelease.com

K2M Introduces Balance ACS™: A Platform of Products, Services & Research Applying Three-Dimensional Solutions to Improve Quality Patient Outcomes for Spine Patients

LEESBURG, Va., Feb. 15, 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 BalanceTM, today introduced Balance ACSTM (or BACSTM), a comprehensive platform that applies three-dimensional solutions across the entire clinical care continuum to help drive quality outcomes for spine patients. BACS provides solutions focused on achieving balance of the spine by addressing each anatomical vertebral segment with a 360-degree approach of the axial, coronal and sagittal planes, emphasizing Total Body BalanceTM as a critical component to surgical success.

“Balancing the head over the pelvis and lower extremities is the foundation of spine surgery,” stated K2M Chief Medical Officer John P. Kostuik, MD. “The spine is a complex structure that provides both stability and three-dimensional motion. Each spine segment is an independent vertebrae that moves in the axial, coronal and sagittal planes. Movement of each segment is part of the complex integrated network of the comprehensive spine serving to provide balance for the entire body, which enhances energy preservation.”

K2M’s Balance ACS platform provides support to the full continuum of spinal care. As part of this comprehensive platform, K2M has launched the BACS System to provide the necessary services—from preauthorization tools and preoperative planning to 3D anatomical modeling and postoperative reporting—to facilitate quality outcomes and to support the intraoperative process. The Company will also use predictive analytics to aid in surgeon decision making and individualized care solutions for patients.

K2M will host physician workshops and symposiums on Balance ACS at leading spine conferences in the United States and internationally. These workshops will feature prominent spine surgeons presenting on the latest research and clinical applications of the Balance ACS platform.

“Since our inception, K2M has been a leader in developing complex spine innovations, technologies and techniques to treat the most complicated spinal pathologies,” stated K2M President and CEO Eric Major. “However, we recognize that three-dimensional spinal balance, and ultimately Total Body BalanceTM, cannot be achieved through surgical spine implants alone; it requires a holistic approach to enable healthcare providers to manage the entire patient experience throughout the continuum of care. As a leader in three-dimensional deformity correction and 3D-printed spinal implants, we are uniquely positioned to take on this endeavor, and today, are excited to introduce our comprehensive platform for achieving Total Body BalanceTM: Balance ACS.”

An integral part of K2M’s new platform is the advancement of new capabilities to complement the Company’s leadership as an innovator of spinal products. To further enhance the Balance ACS platform, the Company announced a partnership with 3D Systems Corporation (NYSE:DDD), originator of 3D printing and a shaper of future 3D solutions. K2M and 3D Systems have entered into a comprehensive development agreement that includes an exclusive software solutions partnership, as part of the BACS System, to aide in balancing the spine across all three planes. In addition, K2M entered into a separate supply agreement with 3D Systems for production capacity to support the production of its highly successful CASCADIATM Interbody Systems featuring Lamellar 3D Titanium TechnologyTM.

The Company has also acquired the e-FellowTM service-based technology that provides automated solutions to surgeons and healthcare systems to effectively collect real-time data and monitor patient outcomes. The technology is an intuitive and powerful healthcare software platform assisting patients and their physicians in obtaining insurance preauthorization and quantifying patient care.

“Rapid innovation has been essential to K2M’s ability to drive organic growth at above-market rates and has fueled tremendous market share growth since the Company’s inception. With our Balance ACS platform, we recognized the opportunity to leverage our core competency of complex spine and minimally invasive offerings, as well as our leadership in comprehensive 3D-printed solutions, to address the full spectrum of spinal care. We are excited to announce our expanded relationship with 3D Systems—a trusted partner through the development and manufacturing of our CASCADIA Interbody Systems featuring Lamellar 3D Titanium Technology—and look forward to incorporating 3D-printed technology into future product development activities. These strategic initiatives, as well as contributions from our recent e-Fellow technology acquisition, reinforce our dedication to providing spine patients, surgeons and healthcare systems with the products, services and tools needed to achieve a complete patient experience and, ultimately, three-dimensional Total Body BalanceTM,” Major added.

For more information about Balance ACS and K2M, visit www.BACS.com and www.K2M.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 BalanceTM. 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, including with respect to our international distribution partners in Australia and Japan. 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; our ability to successfully demonstrate the merits of our technologies and techniques; pricing pressure from our competitors, hospitals and changes in third-party coverage and reimbursement; competition and our ability to develop and commercialize new products; the greater resources available to some of our competitors; aggregation of hospital purchasing from collaboration and consolidation; hospitals and other healthcare providers may be unable to obtain adequate coverage and reimbursement for procedures performed using our products; the safety and efficacy of our products is not yet supported by long-term clinical data; our 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 our products; the proliferation of physician-owned distributorships; concentration of sales from a limited number of spinal systems or products that incorporate these technologies; loss of the services of key members of our senior management, consultants or personnel; ability to enhance our product offerings through our research and development efforts; failure to properly manage our anticipated growth; acquisitions of or investments in new or complementary businesses, products or technologies; ability to train surgeons on the safe and appropriate use of our products; requirements to maintain high levels of inventory; impairment of our goodwill or intangible assets; disruptions in our information technology systems; any disruption or delays in operations at our facilities, including our new headquarters facility; our ability to ship a sufficient number of our products to meet demand; ability to strengthen our brand; fluctuations in insurance cost and availability; extensive governmental regulation including by the FDA; in the United States and foreign jurisdictions; failure to obtain or maintain regulatory approvals and FDA clearances; requirements for new 510(k) clearances, premarket approvals or new or amended CE Certificates of Conformity; medical device reporting regulations in the United States and foreign jurisdictions; voluntary corrective actions by us or our distribution or other business partners or agency enforcement actions; a recall of our products; withdrawal or restrictions on our products or the discovery of serious safety issues with our products; possible enforcement action if we engage in improper marketing or promotion of our products; the misuse or off-label use of our products; delays or failures in any future clinical trials; our reliance on the performance of third parties who assist us in clinical trials and pre-clinical development; the results of clinical trials; procurement and use of allograft bone tissue; environmental laws and regulations; compliance by us or our sales representatives with FDA regulations or fraud and abuse laws; U.S. legislative or regulatory healthcare reforms; medical device tax provisions in the healthcare reform laws; our need to generate significant sales to become profitable; potential fluctuations in sales volumes and our results of operations over the course of the year; uncertainty in our future capital needs; failure to comply with restrictions in our revolving credit facility; continuing worldwide economic instability; our inability to protect our intellectual property rights; our reliance on patent rights that we either license from others or have obtained through assignments; our patent litigation; the outcome of potential claims that we, our employees, our independent sales agencies or our distributors have wrongfully used or disclosed alleged trade secrets or are in breach of non-competition or non-solicitation agreements with our competitors; potential product liability lawsuits; operating risks relating to our international operations; foreign currency fluctuations; our ability to comply with the Foreign Corrupt Practices Act and similar laws associated with our activities outside the United States; possible conflicts of interest with our large shareholders; increased costs and additional regulations and requirements as a result of becoming a public company; our ability to implement and maintain effective internal control over financial reporting in the future; volatility in our common stock; our current plans not to pay dividends; potential dilution due to our issuance of common stock under our incentive plans, for acquisitions or otherwise; the amount of common stock held by our pre-IPO owners; the impact of anti-takeover provisions in our organizational documents and under Delaware law; our status as an emerging growth company, our ability to use our net operating loss carryforwards; the potential impact of any future acquisitions, mergers, dispositions, joint ventures, investments or other strategic transactions we may make; 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.

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

Osteosynthesis Devices Market is Expected to Reach a Value of USD 9.9 Billion by 2024

The osteosynthesis devices market size is expected to reach a value of USD 9.9 billion by 2024, according to a new report by Grand View Research, Inc. The worldwide prevalence of conditions like osteoporosis and osteomalacia, coupled with heavily occurring road traffic injuries/accidents and sporting injuries support the demand for osteosynthesis devices worldwide.

Osteoporosis, a disease resulting in weakening of bones is responsible for causing more than 8.9 million fractures annually. Forearm, humerus, hip and spine are the most commonly affected areas in patients suffering from the disease. The incidence and economic burden of osteoporosis is increasing worldwide, and patients 65 years old or over are at maximum risk of getting affected.

The geriatric population accounted for 46.2 million in 2014, and is increasingly rising. It is projected that by the year 2060, the number of older population will be twice than that of 2014. The rising incidence of osteoporosis and increasing count of the geriatric population is expected to drive demand for osteosynthesis devices in the coming years.

On the other hand, road traffic deaths are at the focal point of a crisis facing public health and development. The WHO reported that accidents/injuries majorly affect the low- and middle-income countries. Road accidents can cause severe injuries such as broken bones and fractures and requires immediate orthopediccare and attention.

 

READ THE REST HERE

Safe Orthopaedics Offers New Technologies to Treat Traumatic Injuries Due to Osteoporosis or Bone Metastases

February 15, 2017

ERAGNY-SUR-OISE, France–(BUSINESS WIRE)–Regulatory News:

SAFE ORTHOPAEDICS (Paris:SAFOR) (FR0012452746 – SAFOR), a company offering innovative ranges of sterile implants combined with their single-use instruments for back surgery, now offers a transverse connector designed to rigidify the stabilisation of posterior spinal osteosynthesis, as well as cement injectable through the Cypress screw to enhance its anchoring strength in osteoporotic or metastatic bone.

Osteoporosis and bone metastatic disease are associated with reduced bone density, which makes the bone more brittle. Osteoporosis is a widespread condition, affecting mostly people over 65 and post-menopausal women. Also with ageing demographics, the prevalence of spinal fractures is rising.

The injection of cement into the vertebra enhances the anchoring strength of Cypress screws, thereby reducing the risk of postoperative instability and repeat surgery.

Dr Jörg Franke, orthopedic surgeon at the Magdebourg Hospital in Germany and member of the Safe Orthopaedics scientific committee, said: “The solution proposed by Safe Orthopaedics improves considerably the options in Cypress screw fixation, by increasing its anchoring strength irrespective of bone quality, with the added possibility of injecting cement into the vertebra during the procedure.”

Furthermore, with its preassembled instruments, the Safe Orthopaedics solution eliminates the risk of cement leakage as the injection is performed directly into the vertebra through a single-use screwdriver, which would be impossible to do with a reusable screwdriver. The injection of cement directly into a cannula inside the screwdriver’s handle also makes the procedure easier and thus reduces operating time.

Pierre Dumouchel, Chief Executive Officer of Safe Orthopaedics, said: “With these additions to our range, which meet our availability and modularity requirements, we are now able to offer more options to surgeons to treat bone injuries associated with osteoporosis and metastases. Our Oak screw, dedicated to the treatment of spinal fractures, will also be available in a cemetable version this year, to offer simultaneous correction and fixation of osteoporotic vertebral fractures using a percutaneous approach.”

Next report

Full-year 2016 results on April 28, 2017 (after market close)

About Safe Orthopaedics

Founded in 2010, Safe Orthopaedics is a French medical technology company that aims to make spinal surgeries safer by using sterile implants and associated single-use instruments. Through this approach, these products eliminate all risk of contamination, reduce infection risks and facilitate a minimally-invasive approach for trauma and degenerative pathologies—benefiting patients. Protected by 17 patent families, the SteriSpineTM kits are CE-marked and FDA approved. The company is based at Eragny-sur-Oise (Val d’Oise department), and has 30 employees.

For more information, visit: www.SafeOrtho.com

Contacts

Safe Orthopaedics
Thierry Lambert, Tél. : +33 (0)1 34 21 50 00
CFO
investors@safeorthopaedics.com
or
NewCap
Julien Perez / Valentine Brouchot
Investor Relations
Nicolas Merigeau
Media Relations
Tél. : +33 (0)1 44 71 94 94
SafeOrtho@newcap.eu