Bodycad Receives FDA 510(k) Clearance for Personalized Unicompartmental Knee
Bodycad received FDAÂ 510(k) clearance to market the Bodycad Unicompartmental Knee joint reconstruction system....
Bodycad received FDAÂ 510(k) clearance to market the Bodycad Unicompartmental Knee joint reconstruction system....
Integra LifeSciences commenced full commercial launch of the Cadence® Total Ankle in Canada, the U.S. and select EU regions....
Stryker Instruments launched System 8 power tools, including the EZout Powered Acetabular Revision System....
Integra LifeSciences launched the Titan™ Press-Fit Reverse Shoulder for Fracture, a 2-piece stem design that does not require cement for fixation....
DJO Global announced FDA 510(k) clearance to market the Exprt® Revision Hip....
Within 2017, Arthrosurface plans commercial EU launch of an inlay glenoid component for the OVOâ„¢ primary stemless total shoulder....
DePuy Synthes launched the ATTUNE® Revision Fixed Bearing Tibial Base and 14x50mm Cemented Stem. ...
Study results demonstrate the clinical and economic value of DePuy Synthes’ ATTUNE® knee in a healthcare environment experiencing cost constraint...
Consensus Orthopedics and the University of Miami Health launched a collaborative clinical study to evaluate the recovery effectiveness of acute...
Lima Corporate marked the 10th anniversary of its proprietary 3D printing technology, Trabecular Titanium (TT), initially used on the Lima...
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