WMT IMPLANTABLE K-WIRE

WMT IMPLANTABLE K-WIRE is an FDA 510(k)-cleared medical device (K132895) 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 October 22, 2013. Regulation: 8.