
Biomet Manufacturing Corp
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TITANIUM FEMORAL KNEE COMPONENTS (MAXIM AND AGC) is an FDA 510(k)-cleared medical device (K041466) manufactured by Biomet Manufacturing Corp. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 30, 2004. Regulation: 8.