meddevicedb.com FDA Device Reference

CEREC BLOCS C IN

K123952 Class II Traditional
Decision Date
2013-03-20
Sponsor / Applicant
Sirona Dental Systems GmbH

Technical Specification

510(k) Submission ID K123952
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2013-03-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CEREC BLOCS C IN received FDA 510(k) clearance under submission number K123952, 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 2013-03-20.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.