INTRAMEDULLARY HIP SCREW (MODIFICATION)

INTRAMEDULLARY HIP SCREW (MODIFICATION) is an FDA 510(k)-cleared medical device (K954712) manufactured by Smith & Nephew Richards, 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 October 30, 1995. Regulation: 8.