Expanded FDA 510(k) for First Ray Stealth Staple
First Ray received FDA 510(k) clearance for additional sizes and materials in the Stealth Staple™ line....
First Ray received FDA 510(k) clearance for additional sizes and materials in the Stealth Staple™ line....
Within 2017, Arthrosurface plans commercial EU launch of an inlay glenoid component for the OVOâ„¢ primary stemless total shoulder....
Soft Tissue Regeneration closed a US $1.5MM Series C Financing and rebranded as Biorez. ...
DePuy Synthes launched the ATTUNE® Revision Fixed Bearing Tibial Base and 14x50mm Cemented Stem. ...
Study results indicate that Rotation Medical’s collagen-based Bioinductive Implant induced new tissue formation in all study participants with large and massive...
Studies suggest that a single injection of Mesenchymal Precursor Cells resulted in meaningful improvements in chronic low back pain and function...
SpinalCyte announced the first injection in a clinical trial of CybroCell fibroblasts for spinal disc regeneration....
Medtronic received FDA 510(k) clearance of Kyphon™ Xpede Bone Cement for fixation of pathological fractures of the sacral ala using sacroplasty....
Study results demonstrate the clinical and economic value of DePuy Synthes’ ATTUNE® knee in a healthcare environment experiencing cost constraint...
Strategic orthopaedic-related 510(k)s issued in February 2017 include:Â NanoFuse (Amend Surgical*), Arrowhead Mini-Rail Fixator (Arrowhead), Expandable Interbody System (Atlas Spine), DCM...
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