GUIDE WIRES FOR CANNULATED SCREWS

GUIDE WIRES FOR CANNULATED SCREWS is an FDA 510(k)-cleared medical device (K963432) manufactured by Orthopaedic Biosystems, 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 November 12, 1996. Regulation: 8.