
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
COMPRESS DISTAL FEMORAL REPLACEMENT is an FDA 510(k)-cleared medical device (K031804) manufactured by Biomet, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 2003. Regulation: 8.