FEMORAL PROXIMAL DIAGNOSAL SCREW, FEMORAL TRANSVER

FEMORAL PROXIMAL DIAGNOSAL SCREW, FEMORAL TRANSVER is an FDA 510(k)-cleared medical device (K852026) manufactured by Warsaw Orthopedic, 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 May 21, 1985. Regulation: 8.