ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW

ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW is an FDA 510(k)-cleared medical device (K981858) manufactured by Atlantis Components, 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 March 21, 1999. Regulation: 8.