Zimmer Biomet voluntarily recalled various legacy Biomet products due to cleaning processes that could lead to elevated bacterial endotoxin and residual debris.
Zimmer Biomet (ZBH) received FDA 510(k) clearance for compatibility of the Nexel™ Total Elbow with the Comprehensive® Segmental Revision System. This marks the 1st submission by ZBH to establish compatibility of two separate ZBH implant systems.
Lima Corporate entered into an Innovation Alliance Agreement with the Hospital for Special Surgery. New product co-developments include a Trabecular Titanium total elbow and an advanced acetabular cup.
Our site uses cookies to allow easier access for Members and subscribers and to improve our site. You agree to our use of cookies by closing this message box or continuing to use our site.OkRead more