AMK TOTAL KNEE SYSTEM W/DU PONT ENHANCED UHMWPE

AMK TOTAL KNEE SYSTEM W/DU PONT ENHANCED UHMWPE is an FDA 510(k)-cleared medical device (K910992) manufactured by Depuy, 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 August 9, 1992. Regulation: 8.