meddevicedb.com FDA Device Reference

Kontact Dental Implant System

K213997 Class II Traditional
Decision Date
2022-07-15
Sponsor / Applicant
Biotech Dental, Sas

Technical Specification

510(k) Submission ID K213997
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2022-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Kontact Dental Implant System received FDA 510(k) clearance under submission number K213997, sponsored by Biotech Dental, Sas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2022-07-15.

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.