DEPUY AMK 3 PEG PATELLA

DEPUY AMK 3 PEG PATELLA is an FDA 510(k)-cleared medical device (K972643) 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 January 20, 1998. Regulation: 8.