METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM

METAGEN ACTIVELOCK WIRE CERCLAGE SYSTEM is an FDA 510(k)-cleared medical device (K983976) 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 December 29, 1998. Regulation: 8.