Clearance Summary
STERI-OSS TEMPORARY IMPLANT CEMENT received FDA 510(k) clearance under submission number K963078, 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 1996-09-10.
- Submission: K963078
- Applicant / Sponsor: Steri-Oss, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3275
- Decision date: 1996-09-10
Classification & Regulation
This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.