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IMPLANT HANDPIECES

K051661 Class I Traditional
Decision Date
2005-09-06
Sponsor / Applicant
Sirona Dental Systems GmbH

Technical Specification

510(k) Submission ID K051661
Product Code EKX
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2005-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPLANT HANDPIECES received FDA 510(k) clearance under submission number K051661, sponsored by Sirona Dental Systems GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-09-06.

Classification & Regulation

This clearance is catalogued under FDA product code EKX and 21 CFR 872.4200, within the Dental review panel as a Class I device.