TITANIUM CANNULATED TIBIAL NAIL (TI CTN)

TITANIUM CANNULATED TIBIAL NAIL (TI CTN) is an FDA 510(k)-cleared medical device (K962047) 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 July 23, 1996. Regulation: 8.