SYNTHES PROXIMAL FEMORAL NAIL(PFN) SYSTEM MODIFICATION

SYNTHES PROXIMAL FEMORAL NAIL(PFN) SYSTEM MODIFICATION is an FDA 510(k)-cleared medical device (K973240) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 19, 1997. Regulation: 8.