ACTIVELOCK MODULAR FEMORAL HIP SYSTEM

ACTIVELOCK MODULAR FEMORAL HIP SYSTEM is an FDA 510(k)-cleared medical device (K980020) manufactured by Metagen, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 2, 1998. Regulation: 8.