meddevicedb.com FDA Device Reference

W Zirconia Implants

K172668 Class II Traditional
Decision Date
2018-11-06
Sponsor / Applicant
Tav Medical , Ltd.

Technical Specification

510(k) Submission ID K172668
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2018-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

W Zirconia Implants received FDA 510(k) clearance under submission number K172668, sponsored by Tav Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2018-11-06.

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.