POROUS APF/MODULAR FEMORAL COMPONENT

POROUS APF/MODULAR FEMORAL COMPONENT is an FDA 510(k)-cleared medical device (K852585) 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 21, 1985. Regulation: 8.