HOWMEDICA MODULAR REPLACEMENT SYSTEM-PROXIMAL FEMUR

HOWMEDICA MODULAR REPLACEMENT SYSTEM-PROXIMAL FEMUR is an FDA 510(k)-cleared medical device (K965164) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 1997. Regulation: 8.