meddevicedb.com FDA Device Reference

CERAMAGE

K050401 Class II Traditional
Decision Date
2005-04-28
Sponsor / Applicant
Shofu Dental Corp.

Technical Specification

510(k) Submission ID K050401
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2005-04-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CERAMAGE received FDA 510(k) clearance under submission number K050401, sponsored by Shofu Dental Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-04-28.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.