SYNTHES TITANIUM DIASTAL FEMORAL NAIL (TI DFN) SYSTEM

SYNTHES TITANIUM DIASTAL FEMORAL NAIL (TI DFN) SYSTEM is an FDA 510(k)-cleared medical device (K970733) 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 April 1, 1997. Regulation: 8.