OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL

OSTEO IC RETROGRADE/ANTEGRADE FEMORAL NAIL is an FDA 510(k)-cleared medical device (K982601) manufactured by Osteonics Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 13, 1998. Regulation: 8.