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FRIALIT-2 ESTHETICBASE ABUTMENT

K013438 Class II Traditional
Decision Date
2001-12-20
Sponsor / Applicant
Friadent GmbH

Technical Specification

510(k) Submission ID K013438
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2001-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRIALIT-2 ESTHETICBASE ABUTMENT received FDA 510(k) clearance under submission number K013438, sponsored by Friadent GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2001-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.