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Biomet Receives FDA Clearance for Two Shoulder Products

Written by  Laura Miller | January 12, 2012
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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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