REGENEROSS ALLOGRAFT PLUS MINERLIZED

REGENEROSS ALLOGRAFT PLUS MINERLIZED is an FDA 510(k)-cleared medical device (K113645) manufactured by Biomet Interpore Cross. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 19, 2012. Regulation: 8.