INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE

INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE is an FDA 510(k)-cleared medical device (K972842) manufactured by Interpore Intl.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 29, 1997. Regulation: 8.