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MTA ROOT CANAL SEALER

K080203 Class II Traditional
Decision Date
2008-03-26
Sponsor / Applicant
Dentsply Interntional

Technical Specification

510(k) Submission ID K080203
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2008-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTA ROOT CANAL SEALER received FDA 510(k) clearance under submission number K080203, sponsored by Dentsply Interntional. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-03-26.

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.