TRUE/FLEX HUMERUS, ULNA AND RADIUS INTRAMEDULLARY

TRUE/FLEX HUMERUS, ULNA AND RADIUS INTRAMEDULLARY is an FDA 510(k)-cleared medical device (K902264) manufactured by Applied Osteo Systems, 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 11, 1990. Regulation: 8.