FX-CABLELOK SYSTEM, MODIFICATION

FX-CABLELOK SYSTEM, MODIFICATION is an FDA 510(k)-cleared medical device (K915259) manufactured by Biodynamic Technologies, 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 February 6, 1992. Regulation: 8.