IMZ 2000 INTERLOCK 12/3 - SCREW

IMZ 2000 INTERLOCK 12/3 - SCREW is an FDA 510(k)-cleared medical device (K963522) manufactured by Imz, GmbH. 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 2, 1997. Regulation: 8.