BROOKER BIO-GROOVE FEMORAL COMPONENT

BROOKER BIO-GROOVE FEMORAL COMPONENT is an FDA 510(k)-cleared medical device (K864085) 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 27, 1987. Regulation: 8.