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PROROOT MTA WHITE, PROROOT MTA GRAY

K142178 Class II Traditional
Decision Date
2015-02-26
Sponsor / Applicant
Dentsply International, Inc.

Technical Specification

510(k) Submission ID K142178
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2015-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROROOT MTA WHITE, PROROOT MTA GRAY received FDA 510(k) clearance under submission number K142178, sponsored by Dentsply International, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-02-26.

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.