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STERI-OSS UNTIL IMPLANT CEMENT

K972965 Class II Traditional
Decision Date
1997-11-07
Sponsor / Applicant
Steri-Oss, Inc.

Technical Specification

510(k) Submission ID K972965
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 1997-11-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERI-OSS UNTIL IMPLANT CEMENT received FDA 510(k) clearance under submission number K972965, 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 1997-11-07.

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.