BONESOURCE HYDROXYAPATITE CEMENT (HAC)

BONESOURCE HYDROXYAPATITE CEMENT (HAC) is an FDA 510(k)-cleared medical device (K953339) manufactured by Osteogenics, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 26, 1996. Regulation: 8.