SYNTHES LCP PROXIMAL TIBIA PLATES LINE EXTENSION

SYNTHES LCP PROXIMAL TIBIA PLATES LINE EXTENSION is an FDA 510(k)-cleared medical device (K052390) manufactured by Synthes (Usa). 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 6, 2005. Regulation: 8.