FIXION INTRAMEDULLARY NAILING SYSTEM

FIXION INTRAMEDULLARY NAILING SYSTEM is an FDA 510(k)-cleared medical device (K990717) manufactured by Disco-O-Tech Medical Technologies, Ltd.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 1, 1999. Regulation: 8.