PROXIMAL FEMORAL REPLACEMENT PROSTHESIS

PROXIMAL FEMORAL REPLACEMENT PROSTHESIS is an FDA 510(k)-cleared medical device (K874575) manufactured by Dow Corning Wright. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 1988. Regulation: 8.