meddevicedb.com FDA Device Reference

CDC ZIRCONIA BLANKS

K122972 Class II Traditional
Decision Date
2012-10-24
Sponsor / Applicant
Continental Dental Ceramics, Inc. (Dba Continental

Technical Specification

510(k) Submission ID K122972
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2012-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CDC ZIRCONIA BLANKS received FDA 510(k) clearance under submission number K122972, sponsored by Continental Dental Ceramics, Inc. (Dba Continental. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-10-24.

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.