Xtant Medical Announces First Surgical Cases of Xspan™ Laminoplasty Fixation System

BELGRADE, Mont., Nov. 14, 2016 (GLOBE NEWSWIRE) — Xtant Medical Holdings, Inc. (NYSE MKT:XTNT), a leader in the development of regenerative medicine products and medical devices, today announced the first surgical cases of the Xspan Laminoplasty Fixation System.

The first two cases were performed by Dr. Francisco Vaz-Guimaraes at the Michael E. DeBakey VA Medical Center in Houston. The open door laminoplasty procedure was performed to treat spinal stenosis without fusing the vertebrae. “The Xspan system is easy to put in, final construct was rock solid. Both patients were discharged shortly after the procedure,” stated Dr. Vaz-Guimaraes. Dr. Vaz-Guimaraes is a Neurosurgeon and faculty member at Baylor College of Medicine, and contracted with the Michael E. DeBakey VA Medical Center in Houston.

Dr. Fuentes and Dr. Ehni, both of the VA Medical Center in Houston, advised from concept to final implant, ensuring Xspan was designed utilizing the expertise of surgeons who routinely perform laminoplasty procedures with the expertise of Xtant Medical engineers. “The Xspan Laminoplasty System has been designed to make the open door laminoplasty technique safer, more adaptable to spondylotic variations in the dorsal element anatomy, and simpler to perform,” said Dr. Ehni.

Dr. David Kirschman, developer of Xspan and member of the Xtant Medical Board of Directors, states, “The Xspan system is a comprehensive set of implants and instruments to perform the cervical laminoplasty procedure. This procedure allows for direct decompression of the cervical spine, with minimum disruption to patient anatomy. This system is emblematic of Xtant’s vision to maximize outcomes while minimizing patient impact.”

The Xspan System represents the latest generation of laminoplasty fixation. Spinal laminoplasty is a surgical procedure performed to remove pressure from the spinal cord. Unlike a laminectomy, where the entire lamina is removed and often is performed in conjunction with spinal fusion, laminoplasty involves only an opening or window made on one side of the lamina to alleviate the compression of the spinal cord. The lamina is then restructured by a small plate which allows for an expansion of the spinal canal without losing stability or movement in the vertebrae. This procedure can be completed at single or multiple levels.

Xtant Medical estimates the worldwide market for laminoplasty at $128M and growing. Xspan is currently available to a limited number of key surgeons with a larger general release to follow later in 2017.

About Xtant Medical Holdings

Xtant Medical develops, manufactures and markets regenerative medicine products and medical devices for domestic and international markets. Xtant Medical products serve the specialized needs of orthopedic and neurological surgeons, including orthobiologics for the promotion of bone healing, implants and instrumentation for the treatment of spinal disease, tissue grafts for the treatment of orthopedic disorders, and biologics to promote healing following cranial, and foot and ankle surgeries. With core competencies in both biologic and non-biologic surgical technologies, Xtant Medical can leverage its resources to successfully compete in global neurological and orthopedic surgery markets. For further information, please visit www.xtantmedical.com.

Important Cautions Regarding Forward-looking Statements

This press release contains certain disclosures that may be deemed forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to significant risks and uncertainties. Forward-looking statements include statements that are predictive in nature, that depend upon or refer to future events or conditions, or that include words such as “continue,” “efforts,” “expects,” “anticipates,” “intends,” “plans,” “believes,” “estimates,” “projects,” “forecasts,” “strategy,” “will,” “goal,” “target,” “prospects,” “potential,” “optimistic,” “confident,” “likely,” “probable” or similar expressions or the negative thereof. Statements of historical fact also may be deemed to be forward-looking statements. We caution that these statements by their nature involve risks and uncertainties, and actual results may differ materially depending on a variety of important factors, including, among others: our ability to integrate the acquisition of X-spine Systems, Inc. and any other business combinations or acquisitions successfully; our ability to remain listed on the NYSE MKT; our ability to obtain financing on reasonable terms; our ability to increase revenue; our ability to comply with the covenants in our credit facility; our ability to maintain sufficient liquidity to fund our operations; the ability of our sales force to achieve expected results; our ability to remain competitive; government regulations; our ability to innovate and develop new products; our ability to obtain donor cadavers for our products; our ability to engage and retain qualified technical personnel and members of our management team; the availability of our facilities; government and third-party coverage and reimbursement for our products; our ability to obtain regulatory approvals; our ability to successfully integrate recent and future business combinations or acquisitions; our ability to use our net operating loss carry-forwards to offset future taxable income; our ability to deduct all or a portion of the interest payments on the notes for U.S. federal income tax purposes; our ability to service our debt; product liability claims and other litigation to which we may be subjected; product recalls and defects; timing and results of clinical studies; our ability to obtain and protect our intellectual property and proprietary rights; infringement and ownership of intellectual property; our ability to remain accredited with the American Association of Tissue Banks; influence by our management; our ability to pay dividends; our ability to issue preferred stock; and other factors.

Additional risk factors are listed in the Company’s Annual Report on Form 10-K and Quarterly Reports on Form 10-Q under the heading “Risk Factors.” You should carefully consider the trends, risks and uncertainties described in this document, the Form 10-K and other reports filed with or furnished to the SEC before making any investment decision with respect to our securities. If any of these trends, risks or uncertainties actually occurs or continues, our business, financial condition or operating results could be materially adversely affected, the trading prices of our securities could decline, and you could lose all or part of your investment. The Company undertakes no obligation to release publicly any revisions to any forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events, except as required by law. All forward-looking statements attributable to us or persons acting on our behalf are expressly qualified in their entirety by this cautionary statement.

Investor Contact
CG CAPITAL
Rich Cockrell
877.889.1972
xtant@cg.capital

Company Contact
Xtant Medical
Molly Mason
mmason@xtantmedical.com

First-ever functional, patient-specific hip replacement procedures performed in the USA

14 November 2016

Corin is excited to announce that during the week of November 7, the first-ever functional, patient specific hip replacement procedures were performed using its Optimized Positioning System (OPS™).  Corin’s OPS™ is the first FDA-cleared technology to help surgeons achieve functional, patient-specific component alignment in total hip replacement.

“Corin’s OPS™ technology optimizes the orientation of each individual patient’s acetabular component by incorporating functional assessments into the planning phase. The system allows surgeons to understand the biomechanics of each patient’s pelvis during daily activities, creating the critical inputs required to optimize surgical outcomes and streamline procedural workflows,” said Jim Pierrepont, PhD, Corin’s Head of Technology.

During the course of the week over 25 OPS™ surgeries were performed at ten centers by Dr Steven Barnett of Orthopaedic Specialty Institute in Orange County, CA; Dr Michael Bradley of South County Orthopaedics in Wakefield, RI; Dr H. John Cooper of New York Orthopaedics in New York, NY; Dr Todd Kelley of University of Cincinnati in Cincinnati, OH; Dr Stefan Kreuzer of Inov8 Orthopaedics in Houston, TX; Dr Michael Miranda and Dr David Watson of Florida Orthopaedic Institute in Temple Terrace, FL; Dr Stephen Raterman of Florida Medical Clinic in Tampa, FL, Dr Herrick Siegel of University of Alabama in Birmingham, AL; Dr Michael Swank of Reconstructive Orthopaedics and Sports Medicine in Cincinnati, OH; and Dr Jonathan Vigdorchik of NYU Hospital for Joint Disease in New York, NY.

“OPS™ and functional component positioning represent a necessary paradigm shift in orthopaedics.  While we have made great progress making surgery less invasive, we have been on a quest for a better way to place components based on individual patients’ needs. Until now, we have based our knowledge of implant position on a 30-year-old publication, which has recently been challenged with data from institutions such as The Mayo Clinic in Rochester, MN and The Hospital for Special Surgery (HSS) in New York,” explained Dr Stefan Kreuzer.

Dr Michael Miranda added, “OPS™ is the first available system that takes us forward in understanding and addressing functional implant positioning. I am very excited to have access to this innovation to help me individualize every patient’s surgery by optimizing implant positioning to improve clinical outcomes.”

“Combined with Corin’s leading portfolio of hip, knee, and extremities prostheses and rapidly expanding global footprint, OPS™ provides a strong foundation for future growth. OPS™ represents Corin’s ongoing commitment to deliver solutions that matter to our surgeon customers and their patients,” said Paul Berman, Corin’s US President.

Minimus Spine Enrolls 30th Subject to Randomized Study Comparing Triojection® to Discectomy

November 14, 2016

Minimus Spine, the developer and manufacturer of the Triojection System, a novel system intended to facilitate the treatment of disc herniations with an intradiscal injection of ozone gas, announced that it has enrolled the 30th subject into its 50-patient randomized study comparing Triojection to discectomy.

“This is the first study to randomize patients between an intradiscal ozone injection and surgery. Hitting this enrollment milestone puts Minimus in position to complete enrollment by September of next year, resulting in primary endpoint data completed near the end of Q1-2018.”, said David Hooper, PhD, Minimus Spine’s Chief Executive Officer. “Triojection already has CE Mark, and if the product demonstrates comparable outcomes to surgery, Minimus will be well-positioned to expand launch activities in Europe. We recognize that new products must be supported with rigorous clinical data to justify their cost. There are no short cuts and that is why we have been pro-actively investing in this study.”

Bruce Frankel MD, Professor of Neurosurgery at the Medical University of South Carolina and CoDirector of the MUSC Spine Center, added “Triojection has the potential to significantly impact the treatment of patients with disc herniations. The benefits of epidural steroid injections are limited and the injections simply do not work for everyone. Discectomy is the gold-standard for patients that have not responded to epidural injections or want more immediate benefit. If Triojection can offer a comparable outcome to surgery, then I envision it being used routinely before considering surgery. Triojection would be more attractive to patients and significantly reduce the cost of care. I am looking forward to the results from this study.”

The study is listed on clinicaltrials.gov under identifier NCT02525120. Patients with a confirmed disc herniation and significant leg pain lasting more than 6 weeks are being presented with the option to enroll in the study. Upon consent, patients are randomized in a 1:1 ratio between Triojection and discectomy. The primary outcome is non-inferiority of Triojection to discectomy surgery for improvement in leg pain over six month following treatment. Back pain, disability and other outcomes are also being collected. While the primary endpoint is based on data up to and including six months, Minimus Spine is following these patients for two years. Clinical sites are in Italy, Switzerland and Greece.

 

About Minimus Spine:

Established in 2006, Minimus Spine is a privately held medical device company dedicated to developing the Triojection technology the non-surgical treatment of herniated discs. Minimus Spine maintains its headquarters in Austin, TX. For more information on Minimus Spine, please visit www.minimusspine.com or email info@minimusspine.com

DJO Global Announces Appointment of Brady Shirley as President and Chief Executive Officer

November 14, 2016

SAN DIEGO–(BUSINESS WIRE)–DJO Global, Inc., a leading global provider of medical technologies designed to get and keep people moving, announced the appointment of Brady Shirley as President and Chief Executive Officer, effective immediately. Mr. Shirley will succeed Mike Mogul, DJO’s current President and Chief Executive Officer who informed the Board of his intent to step down effective November 14, 2016 and will stay on until the end of the year to ensure a smooth transition.

“We are delighted to announce the appointment of Brady Shirley as President and Chief Executive Officer. Since Brady joined DJO, the surgical business has more than doubled in revenue and profitability,” said Mike Zafirovski, DJO’s Chairman of the Board of Directors. “The Board unanimously agrees that Brady’s leadership experience, coupled with his innovative and strategic thinking and proven track record of delivering results, make him the right person to drive DJO’s dual imperatives of achieving sustainable above market growth and driving cost and service leadership in all of our activities.”

Mr. Shirley most recently served as the President of our DJO Surgical business, a position he was appointed to in March of 2014. From 2009 to 2013, Mr. Shirley was the CEO and Director of Innovative Medical Device Solutions (“IMDS”), a company that provides comprehensive product development, manufacturing and supply chain management solutions for medical devices companies within the orthopedic medical device industry. At IMDS, Mr. Shirley managed the integration of four companies, consolidated the capital structure and led a successful sale of the business in 2013. From December 1992 to August 2009, Mr. Shirley had several key leadership positions with Stryker Corporation, including President of Stryker Communications and Senior Vice President of Stryker Endoscopy. At Stryker, Mr. Shirley was responsible for all domestic operations and profit and loss for the Communications division and was responsible for global product development and sales and marketing for the Endoscopy division. Mr. Shirley received a Bachelor of Business Administration in Finance from the University of Texas, Austin.

“I am honored and excited to lead DJO through what I would consider to be a unique evolution. Our fast growing surgical business, our market leading bracing and vascular business and rapidly expanding consumer business create a broad base for expansive revenue growth and operational productivity today and tomorrow,” said Mr. Shirley.

“We would like to take this opportunity to thank Mike for his many contributions over the past 5 years. Under his leadership, DJO has grown significantly faster than our competitors, and our new product innovation has increased four-fold. I also want to commend Mike for helping recruit and develop many talented leaders in the company, which will serve us well in the future,” said Mr. Zafirovski.

“I am proud of how our team has created a company that is building a bright future, spanning the episode of orthopedic care, leading in its markets and realizing the vision of Motion is Medicine,” said Mr. Mogul. “I am convinced that Brady and the strong team that he will lead will demonstrate the great impact that DJO can make.”

About DJO Global

DJO Global is a leading global provider of medical technologies designed to get and keep people moving. The Company’s products address the continuum of patient care from injury prevention to rehabilitation after surgery, injury or from degenerative disease, enabling people to regain or maintain their natural motion. Its products are used by orthopedic specialists, spine surgeons, primary care physicians, pain management specialists, physical therapists, podiatrists, chiropractors, athletic trainers and other healthcare professionals. In addition, many of the Company’s medical devices and related accessories are used by athletes and patients for injury prevention and at-home physical therapy treatment. The Company’s product lines include rigid and soft orthopedic bracing, hot and cold therapy, bone growth stimulators, vascular therapy systems and compression garments, therapeutic shoes and inserts, electrical stimulators used for pain management and physical therapy products. The Company’s surgical division offers a comprehensive suite of reconstructive joint products for the hip, knee and shoulder. DJO Global’s products are marketed under a portfolio of brands including Aircast®, Chattanooga, CMFTM, Compex®, DonJoy®, ProCare®, DJO® Surgical, Dr. Comfort®, Bell-Horn® and ExosTM. For additional information on the Company, please visit www.DJOglobal.com.

Contacts

DJO Investor/Media Contact:
DJO Global, Inc.
Matt Simons
SVP Business Development and Investor Relations
760.734.5548
matt.simons@DJOglobal.com

Bioventus Expands to Mexico with DUROLANE® for Knee Osteoarthritis Patients

November 14, 2016

HOOFDDORP, The Netherlands–(BUSINESS WIRE)–Bioventus, a leader in orthobiologic solutions, has entered the patient care market in Mexico. This announcement reflects the company’s continued growth in international markets and its mission to partner with the health care community to help people resume and enjoy active lives. The initial Bioventus product available in Mexico is DUROLANE a single-injection joint-fluid therapy based on a natural, safe and proven technology called NASHA® which yields stabilized hyaluronic acid (HA). Hyaluronic acid is a naturally occurring molecule that provides the lubrication and cushioning in a normal joint. In Mexico, DUROLANE is indicated for the symptomatic treatment of mild to moderate knee osteoarthritis (OA).

“International expansion is a key part of our growth strategy at Bioventus and launching in Mexico gives us greater access in Latin America which has tremendous potential for us,” said Tony Bihl, CEO, Bioventus. “We now have orthobiologic solutions in more than 29 countries and expect to expand our global sales and marketing footprint even more in the months to come.”

DUROLANE gives patients suffering from knee osteoarthritis another option for pain management,” said Isabelle Levy-Unger, Managing Director International, for Canada, Latin America and Asia Pacific, Bioventus. “It will be sold through Artimedica SA, a Mexican-based company that specializes in the sale and distribution of diagnostic, surgical and other healthcare products for hospitals and clinics across Mexico. We look forward to working with them to introduce this innovative single-injection solution to OA patients throughout the region.”

“We are very excited to market DUROLANE in Mexico,” said Arnulfo Salazar Guerra, Legal Representative for Artimedica. “Its technology offers clear benefits for the estimated 6.7 million Mexican patients that suffer from knee osteoarthritis.”

DUROLANE is available in Mexico now and is part of the Bioventus Active Healing Therapies portfolio which consists of products that allow patients to resume active lives using their bodies own processes to heal faster or reduce pain. More information is available at www.durolane.com.

About Bioventus

Bioventus is an orthobiologics company that delivers clinically proven, cost-effective products that help people heal quickly and safely. Its mission is to make a difference by helping patients resume and enjoy active lives. Bioventus has two product portfolios for orthobiologics, Bioventus Active Healing Therapies and Bioventus Surgical, that make it a global leader in active orthopaedic healing. Built on a commitment to high quality standards, evidence-based medicine and strong ethical behavior, Bioventus is a trusted partner for physicians worldwide.

For more information, visit www.BioventusGlobal.com and follow the company on Twitter @Bioventusglobal.

DUROLANE – Indications

For the symptomatic treatment of mild to moderate knee osteoarthritis.

There are no known contraindications. You should not use DUROLANE if you have infections or skin disease at the injection site. DUROLANE has not been tested in pregnant or lactating women, or children. Risks can include transient pain, swelling and/or stiffness at the injection site. Clinical effectiveness has been demonstrated out to six months but results may vary depending on various patient factors.

NASHA is a registered trademark of Galderma S.A.

Bioventus, the Bioventus logo and DUROLANE are registered trademarks of Bioventus LLC.

Contacts

Media Contacts:
Bioventus
Thomas Hill
+1 919-474-6715
thomas.hill@bioventusglobal.com

Stryker announces multi-year partnership with Indo UK Institute of Health to deliver affordable orthopaedic care in India

Kalamazoo, Michigan – November 14, 2016 – Stryker Corporation (SYK), one of the world`s leading medical technology companies, announced today a multi-year collaboration with Indo UK Institute of Health`s (IUIH) Medicity Program to serve as a preferred partner in the orthopaedic areas of hip, knee, and trauma products and services. Stryker and IUIH`s new relationship will provide greater access to affordable primary joint replacements and other healthcare services to patients in India.

The unprecedented 20-year partnership between Stryker and IUIH, a forward-looking healthcare provider, will create and deliver real value throughout the continuum of orthopaedic care, driven by a combination of Stryker`s quality implants and products, streamlined patient pathways and world-class commercial services.

“We are proud to partner with Indo UK Institute of Health to make quality healthcare more accessible and affordable to the people of India, not only through the broad portfolio of products that we offer but also in our commitment to research and medical education,” said Kevin A. Lobo, Chairman and Chief Executive Officer.

In addition to its commitment to provide access to its joint replacement and trauma products and technology, Stryker`s commitment includes the sponsorship of a post-graduate training and education center on the campus of one of IUIH`s medicities and R&D collaboration with Stryker`s longstanding Global Technology Center in India.

“The partnership with Stryker is set to redefine the existing paradigms in healthcare industry,” said Ajay Rajan Gupta, Managing Director and Group CEO, IUIH. “With predictable orthopaedic spend, improved cash flow and optimized use of technology resources, the agreement with Stryker will enhance IUIH`s value in healthcare space in years to come.”

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; 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; 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.

About Indo UK Institute of Health
On November 12, 2015, the United Kingdom Prime Minister, Mr. David Cameron, and the Prime Minister of India, Mr. Narendra Modi, signed a joint statement to support the development of 11 Indo UK Institutes of Health across 11 states in India. The Indo UK Institute of Health project brings the best of National Health Service (NHS) to India to develop a new healthcare ecosystem which is available, affordable, accountable and appropriate to all. Each Indo UK Institute of Health will have a 1,000 bed NHS hospital, a nursing college, medical college, post graduate training center, implant manufacturing unit, eHealth center and accommodation. Please visit www.iuih.co.uk for more information or contact victoria.lusher@iuih.co.uk.

Expanding Orthopedics Inc. Granted a New US Patent for Its Unique 3D Expandable Cage

OR AKIVA, Israel, November 14, 2016 /PRNewswire/ —

Expanding Orthopedics Inc. (EOI), a privately held medical device company focused on developing and commercializing innovative expandable devices for spine surgery, is excited to announce that it has been granted its 14th US Patent, covering its unique 3D expandable cage technology integrated in the FLXfit™.”

Dr. Mark M. Levy, an orthopedic surgeon, CTO and founder of EOI says that, “This new patent recognizes the unique innovation of our 3D expandable cage, the FLXfit™.” He explains that, “This patent refers to the multiple segments design with its articulation mechanism and the unique angular expansion for dial-in lordosis correction, conforming to the patient’s anatomy and level treated.”

Mr. Ofer Bokobza, EOI’s CEO, commented, “This new patent grant is an important addition to our broad IP portfolio, demonstrating our continuous commitment to innovation and our ability to develop state-of-the-art devices addressing unmet clinical designed to improve patients’ outcome”. He concludes that, “We are working diligently on a rich product pipeline with unique IP which will reinforce our position as a fast growing expandable devices’ spine company.”

About Expanding Orthopedics Inc.

Expanding Orthopedics Inc. (EOI) 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 backed by prominent spine surgeons. EOI owns a broad patent portfolio around anatomically fit, expandable devices for enhanced stability through a minimally invasive approach.

Contact info:
David Elkaim, VP Marketing and Sales
E-mail: david@xortho.com
Phone: +1-347-321-9683

SOURCE Expanding Orthopedics Inc. (EOI)

Titan Spine Appoints Spine Industry Veteran Ted Bird as Chief Commercial Officer

November 14, 2016

MEQUON, Wis.–(BUSINESS WIRE)–Titan Spine, a medical device surface technology company focused on developing innovative spinal interbody fusion implants, today announced Ted Bird has joined the executive management team as Chief Commercial Officer (CCO). Mr. Bird will be responsible for the Company’s global sales, marketing, strategic partnering, and national target accounts.

Peter Ullrich, Chief Executive Officer of Titan Spine, commented, “Ted is a well-respected medical device commercial leader with more than 30 years of sales, marketing and senior executive experience at leading healthcare companies. He is well-known and highly regarded in the spine industry, with extensive relationships among surgeons and distributors built from over 25 years working with spine companies including ApiFix, Orthofix, Depuy Spine and Medtronic Sofamor Danek. We look forward to Ted’s significant spine commercialization expertise and contributions as Titan Spine continues ramping up its full U.S. launch of our Endoskeleton® titanium implants featuring our groundbreaking nanoLOCK® surface technology, the only nano-cleared interbody device on the market shown to elicit a nano-cellular level response for bone growth.”

Mr. Bird added, “I am incredibly excited and honored to be joining the Titan Spine team. The company has been at the forefront of moving the interbody device marketplace away from PEEK and towards titanium surface-enhanced implants for improved patient outcomes with validated, peer-reviewed science and strong support from surgeons, hospitals and the U.S. government. I look forward to working closely with the talented team at Titan Spine to continue building on the positive momentum that the company continues to generate and help lead the next phase of the company’s evolution and growth.”

Prior to joining Titan Spine, Mr. Bird was the non-executive Chairman of the Board for ApiFix, an Israeli start-up company with a minimally invasive, fusion-less technology for correction of early onset and adolescent scoliosis and President of Bird Medical, a strategic consulting firm for healthcare manufacturers. Previously, Mr. Bird successfully led and inspired global business units and commercial teams at Orthofix, including roles as President, Spine Fixation Division, Senior Vice President Global Marketing and Senior Vice President, U.S. Sales; Depuy Spine, including roles of Vice President, Field Marketing & Strategic Development and Vice President of Spine Arthroplasty Education; and Medtronic Sofamor Danek, including roles as Vice President, Global Medical Education and Emerging Technologies and Vice President, Marketing. He started his career in arthroscopy sales at Dyonics and progressed to key marketing positions at Microvasive and Johnson & Johnson Orthopedics. Mr. Bird is a graduate of Brown University with bachelor’s degrees in International Relations and Political Science.

Titan Spine offers a full line of Endoskeleton® devices that feature Titan Spine’s proprietary nanoLOCK® surface technology, consisting of a unique combination of roughened topographies at the macro, micro, and nano levels (MMN™). This unique combination of surface topographies is designed to create an optimal host-bone response and actively participate in the fusion process by promoting the upregulation of osteogenic and angiogenic factors necessary for bone growth, encouraging natural production of bone morphogenetic proteins (BMPs), downregulating inflammatory factors, and creating the potential for a faster and more robust fusion.1,2 All Endoskeleton® devices are covered by the company’s risk share warranty.

About Titan Spine

Titan Spine, LLC is a surface technology company focused on the design and manufacture of interbody fusion devices for the spine. The company is committed to advancing the science of surface engineering to enhance the treatment of various pathologies of the spine that require fusion. Titan Spine, located in Mequon, Wisconsin and Laichingen, Germany, markets a full line of Endoskeleton® interbody devices featuring its proprietary textured surface in the U.S. and portions of Europe through its sales force and a network of independent distributors. To learn more, visit www.titanspine.com.

1 Olivares-Navarrete, R., Hyzy S.L., Gittens, R.A., Berg, M.E., Schneider, J.M., Hotchkiss, K., Schwartz, Z., Boyan, B. D. Osteoblast lineage cells can discriminate microscale topographic features on titanium-aluminum-vanadium surfaces. Ann Biomed Eng. 2014 Dec; 42 (12): 2551-61.

2 Olivares-Navarrete, R., Hyzy, S.L., Slosar, P.J., Schneider, J.M., Schwartz, Z., and Boyan, B.D. (2015). Implant materials generate different peri-implant inflammatory factors: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors. Spine, Volume 40, Issue 6, 399–404.

Contacts

Titan Spine
Andrew Shepherd, 866-822-7800
ashepherd@titanspine.com
or
Media:
The Ruth Group
Kirsten Thomas, 508-280-6592
kthomas@theruthgroup.com

TransEnterix bets on haptics for Senhance robot-assisted surgery device

BY

TransEnterix (NYSE:TRXC) is betting that the haptics technology in its Senhance robot-assisted surgery platform will help it make headway against Intuitive Surgical (NSDQ:ISRG) and its 10-year lead on the market.

CEO Todd Pope told MassDevice.com that the Senhance’s haptics – the system’s ability to convey a sense of touch and resistance to the surgeon – are an important selling point with physicians.

“The 1 thing that they tell us, as far as a feature that they miss the most on robotics, is the sense of feel or touch. When surgeons do open surgery, they rely on their hands and touch a great deal. Even with laparoscopic surgery, they have that tactile feedback. They have none of that with the current robotics systems today,” Pope told us. “Surgeons have told us when they’re dissecting tissue planes, when they’re working around important vessels or organs, often the sense of touch is just as important for them to discern what they want to do next in the surgery as anything else.”

The TransEnterix haptics tech works on the concept of force feedback, he explained. Senhance’s interaction with tissue is fed back as haptic force to the surgeon’s hands. In demos of the system, surgeons are able to knot a suture while blindfolded, Pope said.

“We had so many surgeons that are using the Senhance say that it was enhancing their senses, it was taking their sense of feel, their sense of touch, and, certainly, their sense of sight and really enhancing it,” he said.

 

READ THE REST HERE

Xtant Medical Reminds Shareholders of Upcoming Expiration of Rights Offering Subscription Period and Final Subscription Price

BELGRADE, Mont., Nov. 11, 2016 (GLOBE NEWSWIRE) — Xtant Medical Holdings, Inc. (NYSE MKT:XTNT), a leader in the development, manufacturing and marketing of orthopedic products for domestic and international markets, reminds rights holders that the subscription period for its previously announced rights offering expires at 5:00 PM Eastern Time on Monday, November 14, 2016. The rights offering is for up to 15,000,000 units, each consisting of one share of common stock and one warrant to purchase one share of common stock. The subscription price is $0.75 per unit, and there will be no further adjustments to the subscription price.

If exercising subscription rights through a broker, dealer, bank or other nominee, rights holders should promptly contact their nominee and submit subscription documents and payment for the units subscribed for in accordance with the instructions and within the time period provided by such nominee. The broker, dealer, bank or other nominee may establish a deadline before November 14, 2016 by which instructions to exercise subscription rights, along with the required subscription payment, must be received.

All holders of rights that wish to participate in the rights offering must deliver by mail, hand or overnight courier, a properly completed and signed subscription rights statement, together with payment of the subscription price for both basic subscription rights and any over subscription privilege election, to the Subscription Agent, to be received before 5:00 PM Eastern Time on November 14, 2016. The Subscription Agent is:

Corporate Stock Transfer, Inc.

3200 Cherry Creek Drive South, Suite 430

Denver, Colorado 80209

Under the proposed rights offering, the Company has distributed two non-transferable subscription rights for each share of common stock held, or underlying convertible notes held, on the record date. Each subscription right entitles the holder to purchase one unit at the subscription price of $0.75 per unit. Each unit consists of one share of common stock and one warrant, with each warrant exercisable to purchase one share of common stock at an exercise price of $0.90 for five years from the date of issuance. After the one-year anniversary of issuance, the Company may redeem the warrants for $0.01 per warrant if the volume weighted average price of the Company’s common stock is greater than $2.25 for each of 10 consecutive trading days.

Holders who exercise their subscription rights in full will be entitled, if available, to subscribe for additional units that are not purchased by other shareholders or convertible note holders, on a pro rata basis and subject to ownership limitations.

Xtant Medical has engaged Maxim Group LLC as dealer-manager in the offering. The offering may only be made by means of a prospectus. Questions about the rights offering or requests for copies of the prospectus may be directed to:

Maxim Group LLC

405 Lexington Avenue

New York, NY 10174

Attention: Syndicate Department

Email: syndicate@maximgrp.com

Telephone: (212) 895-3745.

The Company’s registration statement on Form S-1 was declared effective by the U.S. Securities and Exchange Commission (SEC) on October 31, 2016. The prospectus relating to and describing the terms of the rights offering has been filed with the SEC as a part of the registration statement and is available on the SEC’s web site at http://www.sec.gov.

This press release does not constitute an offer to sell or the solicitation of an offer to buy these securities, nor will there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

About Xtant Medical Holdings

Xtant Medical Holdings, Inc. (NYSE MKT:XTNT) develops, manufactures and markets class-leading regenerative medicine products and medical devices for domestic and international markets. Xtant products serve the specialized needs of orthopedic and neurological surgeons, including orthobiologics for the promotion of bone healing, implants and instrumentation for the treatment of spinal disease, tissue grafts for the treatment of orthopedic disorders, and biologics to promote healing following cranial, and foot and ankle surgeries. With core competencies in both biologic and non-biologic surgical technologies, Xtant can leverage its resources to successfully compete in global neurological and orthopedic surgery markets. For further information, please visit www.xtantmedical.com.

Important Cautions Regarding Forward-looking Statements

This press release contains certain disclosures that may be deemed forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to significant risks and uncertainties. Forward-looking statements include statements that are predictive in nature, that depend upon or refer to future events or conditions, or that include words such as “continue,” “efforts,” “expects,” “anticipates,” “intends,” “plans,” “believes,” “estimates,” “projects,” “forecasts,” “strategy,” “will,” “goal,” “target,” “prospects,” “potential,” “optimistic,” “confident,” “likely,” “probable” or similar expressions or the negative thereof.

Statements of historical fact also may be deemed to be forward-looking statements. We caution that these statements by their nature involve risks and uncertainties, and actual results may differ materially depending on a variety of important factors, including, among others: our ability to integrate the acquisition of X-spine Systems, Inc. and any other business combinations or acquisitions successfully; our ability to remain listed on the NYSE MKT; our ability to obtain financing on reasonable terms; our ability to increase revenue; our ability to comply with the covenants in our credit facility; our ability to maintain sufficient liquidity to fund our operations; the ability of our sales force to achieve expected results; our ability to remain competitive; government regulations; our ability to innovate and develop new products; our ability to obtain donor cadavers for our products; our ability to engage and retain qualified technical personnel and members of our management team; the availability of our facilities; government and third-party coverage and reimbursement for our products; our ability to obtain regulatory approvals; our ability to successfully integrate recent and future business combinations or acquisitions; our ability to use our net operating loss carry-forwards to offset future taxable income; our ability to deduct all or a portion of the interest payments on the notes for U.S. federal income tax purposes; our ability to service our debt; product liability claims and other litigation to which we may be subjected; product recalls and defects; timing and results of clinical studies; our ability to obtain and protect our intellectual property and proprietary rights; infringement and ownership of intellectual property; our ability to remain accredited with the American Association of Tissue Banks; influence by our management; our ability to pay dividends; our ability to issue preferred stock; and other factors.

Additional risk factors are listed in the Company’s Annual Report on Form 10-K and Quarterly Reports on Form 10-Q under the heading “Risk Factors.” You should carefully consider the trends, risks and uncertainties described in this document, the Form 10-K and other reports filed with or furnished to the SEC before making any investment decision with respect to our securities. If any of these trends, risks or uncertainties actually occurs or continues, our business, financial condition or operating results could be materially adversely affected, the trading prices of our securities could decline, and you could lose all or part of your investment. The Company undertakes no obligation to release publicly any revisions to any forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events, except as required by law. All forward-looking statements attributable to us or persons acting on our behalf are expressly qualified in their entirety by this cautionary statement.

Investor Contact
CG CAPITAL
Rich Cockrell
877.889.1972
xtant@cg.capital

Company Contact
Xtant Medical
Molly Mason
mmason@xtantmedical.com