CITIEFFE-TITANIUM CANNULATED SCREW

CITIEFFE-TITANIUM CANNULATED SCREW is an FDA 510(k)-cleared medical device (K113388) manufactured by Citieffe. 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 4, 2012. Regulation: 8.