Warren, NJ, March 26, 2015 –(PR.com)– NJ-based Prosidyan™ (www.prosidyan.com), developer of proprietary fiber-based bioactive glass products, announced today that it has received FDA 510(k) clearance of FIBERGRAFT™ BG Putty – Bone Graft Substitute. This is the second generation product in
Washington, DC–(ENEWSPF)–April 2, 2015. The Justice Department announced today that Medtronic plc and affiliated Medtronic companies, Medtronic Inc., Medtronic USA Inc., and Medtronic Sofamor Danek USA Inc., have agreed to pay $4.41 million to the United States to resolve allegations
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By Jessica Achtsam On March 31, 2015, Orthofix International N.V. announced it entered into an 18-month option agreement to acquire eNeura, Inc. Orthofix’s website states that the focus of the company is on “improving patients’ lives by providing superior reconstructive and regenerative orthopedic
Although there is a high level of evidence that hip resurfacing arthroplasty preserves bone mineral density and bone stock in the proximal femur, the clinical relevance should be weighed against potential disadvantages, such as a higher revision rate f…
ALLENDALE, N.J., March 25, 2015 /PRNewswire/ — Stryker Corporation’s Spine Division announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the LITe® Plate System, an Anterior and Lateral Lumbar Plate System. The LITe Plate
PLAINSBORO, N.J., April 1, 2015 (GLOBE NEWSWIRE) — Integra LifeSciences Holdings Corporation (Nasdaq:IART) today announced the filing of an initial Form 10 Registration Statement with the Securities and Exchange Commission (“SEC”) in connection with its previously announced plan to spin off SeaSpine
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