
Biomet Manufacturing Corp
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COMPRESS SEGMENTAL FEMORAL REPLACEMENT SYSTEM (SHORT SPINDLE AND ANCHOR PLUG) is an FDA 510(k)-cleared medical device (K062998) manufactured by Biomet Manufacturing Corp. This device is classified under the Orthopedic specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on January 18, 2007. Regulation: 8.