REVERSE CUTTING CANNULATED CANCELLOUS BONE SCREW

REVERSE CUTTING CANNULATED CANCELLOUS BONE SCREW is an FDA 510(k)-cleared medical device (K892214) manufactured by Ace Medical Co.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 21, 1989. Regulation: 8.