PERIOGLAS BONE GRAFT PARTICULATE

PERIOGLAS BONE GRAFT PARTICULATE is an FDA 510(k)-cleared medical device (K053387) manufactured by Novabone Products, LLC. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 13, 2006. Regulation: 8.