DEPUY PROXIMAL FEMORAL REPLACEMENT PROSTHESIS

DEPUY PROXIMAL FEMORAL REPLACEMENT PROSTHESIS is an FDA 510(k)-cleared medical device (K970241) 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 August 13, 1997. Regulation: 8.