ITI SYNOCTA MESO ABUTMENTS

ITI SYNOCTA MESO ABUTMENTS is an FDA 510(k)-cleared medical device (K033243) manufactured by Straumann 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 October 19, 2003. Regulation: 8.