SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM

SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K102656) 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 December 19, 2010. Regulation: 8.