BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS

BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWS is an FDA 510(k)-cleared medical device (K974756) 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 March 11, 1998. Regulation: 8.