MODIFICATION TO TOWNLEY PEDICLE SCREW PLATING SYSTEM

MODIFICATION TO TOWNLEY PEDICLE SCREW PLATING SYSTEM is an FDA 510(k)-cleared medical device (K982686) manufactured by Sofamor Danek USA,Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 6, 1998. Regulation: 8.