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TEMPFX ESTHETIC PROVISIONAL SYSTEM

K061264 Class II Special
Decision Date
2006-05-23
Sponsor / Applicant
Dentsply International, Inc.

Technical Specification

510(k) Submission ID K061264
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2006-05-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEMPFX ESTHETIC PROVISIONAL SYSTEM received FDA 510(k) clearance under submission number K061264, sponsored by Dentsply International, 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 2006-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.