SCREW, BONE, MAXILLOFACIAL

SCREW, BONE, MAXILLOFACIAL is an FDA 510(k)-cleared medical device (K911165) manufactured by Tekno-Medical. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 19, 1991. Regulation: 8.