MAXIM REMOVABLE MOLDED POLY TIBIA

MAXIM REMOVABLE MOLDED POLY TIBIA is an FDA 510(k)-cleared medical device (K991753) 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 August 16, 1999. Regulation: 8.