ANTEGRADE FEMORAL NAIL

ANTEGRADE FEMORAL NAIL is an FDA 510(k)-cleared medical device (K123569) manufactured by Advanced Orthopaedic Solutions, 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 May 23, 2013. Regulation: 8.