meddevicedb.com FDA Device Reference

Zygomatic Implants

K190718 Class II Traditional
Decision Date
2019-07-11
Sponsor / Applicant
Jjgc Industria E Comercio DE Materiais Dentarios S.A.

Technical Specification

510(k) Submission ID K190718
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2019-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Zygomatic Implants received FDA 510(k) clearance under submission number K190718, sponsored by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-07-11.

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.