ODONTIT AUTOGENOUS BONE COLLECTION DEVICE

ODONTIT AUTOGENOUS BONE COLLECTION DEVICE is an FDA 510(k)-cleared medical device (K971036) manufactured by Interpore Intl.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 2, 1997. Regulation: 8.