ATLAS FRACTURE PROXIMAL HUMERAL NAIL

ATLAS FRACTURE PROXIMAL HUMERAL NAIL is an FDA 510(k)-cleared medical device (K971816) manufactured by Biomet, 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 July 17, 1997. Regulation: 8.