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QUATTRO PORCELAIN SYSTEM

K091706 Class II Traditional
Decision Date
2009-08-28
Sponsor / Applicant
Dentsply International, Inc.

Technical Specification

510(k) Submission ID K091706
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2009-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUATTRO PORCELAIN SYSTEM received FDA 510(k) clearance under submission number K091706, 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 2009-08-28.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.