FORCEPS, ANKLE INSERTING, CON-AXIAL

FORCEPS, ANKLE INSERTING, CON-AXIAL is an FDA 510(k)-cleared medical device (K770420) 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 March 13, 1977. Regulation: 8.