Biomet has received FDA 510(k) clearance for two new shoulder products, according to a Biomet news release.
Biomet's E1 humeral bearing for use with the Comprehensive Reverse Shoulder System and the Comprehensive Segmental Revision System both received clearance. The E1 humeral bearing includes antioxidant-infused technology for a Vitamin E advanced bearing. The technology is designed to advance the bearing surface with oxidative stability, high strength and low wear.
The Comprehensive Segmental Revision System is a humeral replacement system designed to address significant bone loss proximally and distally. The system includes oncologic options, soft tissue attachments and several size options.
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The Comprehensive Segmental Revision System is a humeral replacement system designed to address significant bone loss proximally and distally. The system includes oncologic options, soft tissue attachments and several size options.
Related Articles on Orthopedic Device Companies:
38 Orthopedic & Spine Device Company Executive Moves in 2011
Stryker's Preliminary 4Q Report Shows 46.8% Spine & Neurotechnology Sales Increase
Arthrex Partners With ThermoGenesis for PRP System Distribution