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AVANTE Z ZIRCONIA (AS)3 BLOCKS

K081749 Class II Traditional
Decision Date
2008-09-30
Sponsor / Applicant
Pentron Ceramics, Inc.

Technical Specification

510(k) Submission ID K081749
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2008-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AVANTE Z ZIRCONIA (AS)3 BLOCKS received FDA 510(k) clearance under submission number K081749, sponsored by Pentron Ceramics, 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 2008-09-30.

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.