ATLANTIS ABUTMENT FOR STRAUMANN INTERFACE

ATLANTIS ABUTMENT FOR STRAUMANN INTERFACE is an FDA 510(k)-cleared medical device (K050052) 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 6, 2005. Regulation: 8.