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CERAMIR CROWN & BRIDGE

K100510 Class II Special
Decision Date
2010-03-25
Sponsor / Applicant
Doxa AB

Technical Specification

510(k) Submission ID K100510
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2010-03-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CERAMIR CROWN & BRIDGE received FDA 510(k) clearance under submission number K100510, sponsored by Doxa AB. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.