SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM

SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM is an FDA 510(k)-cleared medical device (K063473) manufactured by Synthes (Usa). This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 7, 2007. Regulation: 8.