DARCO HEADED CANNULATED SCREW

DARCO HEADED CANNULATED SCREW is an FDA 510(k)-cleared medical device (K100359) manufactured by Wrightmedicaltechnologyinc. 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 23, 2010. Regulation: 8.