meddevicedb.com FDA Device Reference

CLEARFIL MAJETY POSTERIOR

K100328 Class II Special
Decision Date
2010-03-05
Sponsor / Applicant
Kuraray Medical, Inc.

Technical Specification

510(k) Submission ID K100328
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2010-03-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEARFIL MAJETY POSTERIOR received FDA 510(k) clearance under submission number K100328, sponsored by Kuraray Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-03-05.

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.