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ESTHETIC EASE ABUTMENTS FOR THE ITI DENTAL IMPLANT SYSTEM

K020096 Class II Special
Decision Date
2002-02-08
Sponsor / Applicant
Institut Straumann AG

Technical Specification

510(k) Submission ID K020096
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2002-02-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ESTHETIC EASE ABUTMENTS FOR THE ITI DENTAL IMPLANT SYSTEM received FDA 510(k) clearance under submission number K020096, sponsored by Institut Straumann AG. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-02-08.

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.