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3A DENTAL IMPLANT SYSTEM

K011879 Class II Traditional
Decision Date
2002-08-27
Sponsor / Applicant
Osseco Biosource, Ltd.

Technical Specification

510(k) Submission ID K011879
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2002-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3A DENTAL IMPLANT SYSTEM received FDA 510(k) clearance under submission number K011879, sponsored by Osseco Biosource, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.