
Novabone Products, LLC
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NOVABONE DENTAL PUTTY-BIOACTIVE SYNTHETIC BONE GRAFT is an FDA 510(k)-cleared medical device (K063549) 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 11, 2007. Regulation: 8.