ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS

ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS is an FDA 510(k)-cleared medical device (K073067) manufactured by Dentsply International, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 14, 2008. Regulation: 8.