VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW

VILEX CANNULATED BONE SCREW, DUVAL CANNULATED BONE SCREW is an FDA 510(k)-cleared medical device (K973309) manufactured by Vilex, 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 January 15, 1998. Regulation: 8.