TITANIUIM BONE SCREW

TITANIUIM BONE SCREW is an FDA 510(k)-cleared medical device (K853869) manufactured by George Tiemann & Co.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 8, 1985. Regulation: 8.