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ZIMMER DENTAL TAPERED SWISSPLUS IMPLANTS

K082639 Class II Traditional
Decision Date
2008-12-19
Sponsor / Applicant
Zimmer Dental, Inc.

Technical Specification

510(k) Submission ID K082639
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2008-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZIMMER DENTAL TAPERED SWISSPLUS IMPLANTS received FDA 510(k) clearance under submission number K082639, sponsored by Zimmer Dental, 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 2008-12-19.

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.