STERI-OSS SINUS AUGMENTATION KIT

STERI-OSS SINUS AUGMENTATION KIT is an FDA 510(k)-cleared medical device (K963897) manufactured by Steri-Oss, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 5, 1996. Regulation: 8.