PROGENIX DBM PUTTY

PROGENIX DBM PUTTY is an FDA 510(k)-cleared medical device (K080462) manufactured by Medtronic Sofamor Danek. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 12, 2008. Regulation: 8.