CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM

CANNULATED SCREW AND KIRSCHNER (KWIRE) SYSTEM is an FDA 510(k)-cleared medical device (K130613) manufactured by Laura Cattabriga. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 21, 2014. Regulation: 8.