AGC UNICOMPARTMENTAL KNEE PROSTHESIS

AGC UNICOMPARTMENTAL KNEE PROSTHESIS is an FDA 510(k)-cleared medical device (K873601) 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 January 19, 1988. Regulation: 8.