DEPUY CANNULATED BONE SCREW

DEPUY CANNULATED BONE SCREW is an FDA 510(k)-cleared medical device (K893512) manufactured by Depuy, 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 August 20, 1989. Regulation: 8.