FEMOROTIBIAL MEDULLARY NAIL

FEMOROTIBIAL MEDULLARY NAIL is an FDA 510(k)-cleared medical device (K853250) manufactured by Zimmer, 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 February 11, 1986. Regulation: 8.