SYNTHES MATRIX MIS RODS

SYNTHES MATRIX MIS RODS is an FDA 510(k)-cleared medical device (K093668) 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 March 8, 2010. Regulation: 8.