meddevicedb.com FDA Device Reference

MTA CEMENTS

K130125 Class II Traditional
Decision Date
2013-07-24
Sponsor / Applicant
S&C Polymer Silicon- Und Composite Spezialitaeten

Technical Specification

510(k) Submission ID K130125
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2013-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTA CEMENTS received FDA 510(k) clearance under submission number K130125, sponsored by S&C Polymer Silicon- Und Composite Spezialitaeten. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.