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ENDOSSEOUS IMPLANT

K021355 Class II Traditional
Decision Date
2002-08-30
Sponsor / Applicant
Branemark Integration AB

Technical Specification

510(k) Submission ID K021355
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2002-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSSEOUS IMPLANT received FDA 510(k) clearance under submission number K021355, sponsored by Branemark Integration AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-08-30.

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.