INTRAMEDULLARY BONE PLUG

INTRAMEDULLARY BONE PLUG is an FDA 510(k)-cleared medical device (K832328) manufactured by Kirschner Medical 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 October 19, 1983. Regulation: 8.