Amedica Receives FDA Clearance of Valeo C+CsC
Amedica announced FDA 510(k) clearance of the Valeo C+CsC with Lumen interbody fusion device....
Amedica announced FDA 510(k) clearance of the Valeo C+CsC with Lumen interbody fusion device....
Stryker Spine received FDA 510(k) clearance to market Tritanium® TL, a 3D-printed curved posterior lumbar interbody fusion cage. The device will...
Smith & Nephew launched Q-FIXÂ CURVED, Q-FIX MINI and SUTUREFIX CURVED All-Suture Anchor systems, designed for procedures in difficult-to-access anatomies....
CrossRoads Extremity Systems has launched the DynaFORCE® Active Stabilization Vero Medial Column fixation implant....
Extremity Medical's 2018 product launches will include the Omni foot plating system, AlignX lateral plates for tibiotalar and tibiotalar-calcaneus fusion, Charcot-specific plates...
Globus Medical debuted its FDA-510(k)-cleared trauma products, comprising fracture plates, compression and cannulated screws, intramedullary nails and external fixation. ...
Onkos Surgical signed a 4-year agreement with 3D Systems to develop and advance patient-specific tools for use in tumor-related reconstruction...
Orthofix gained FDA premarket and CE Mark approval for next-gen PhysioStim bone growth stimulators, used as a nonsurgical treatment for nonunion fracture in the extremities....
ulrich medical USA reported 2017 revenue +10% vs. 2016, and a 15% 5-year CAGR for their U.S. spine business....
Stryker launched Pivot Guardian, reportedly the industry's first post-free hip distraction system for arthroscopy. ...
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