DOC VENTRAL CERVICAL STABILIZATION SYSTEM

DOC VENTRAL CERVICAL STABILIZATION SYSTEM is an FDA 510(k)-cleared medical device (K982443) manufactured by Depuy Motech Acromed. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 28, 1998. Regulation: 8.