DEPUY (NITINO) GUIDE WIRE

DEPUY (NITINO) GUIDE WIRE is an FDA 510(k)-cleared medical device (K914693) 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 December 8, 1991. Regulation: 8.