Clearance Summary
STERI-OSS SINUS AUGMENTATION KIT received FDA 510(k) clearance under submission number K963897, sponsored by Steri-Oss, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1996-11-06.
- Submission: K963897
- Applicant / Sponsor: Steri-Oss, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4565
- Decision date: 1996-11-06
Classification & Regulation
This clearance is catalogued under FDA product code EMM and 21 CFR 872.4565, within the Dental review panel as a Class I device.