meddevicedb.com FDA Device Reference

QRS Dental Implants System

K221910 Class II Traditional
Decision Date
2022-12-14
Sponsor / Applicant
Qrs Medical , Ltd.

Technical Specification

510(k) Submission ID K221910
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2022-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QRS Dental Implants System received FDA 510(k) clearance under submission number K221910, sponsored by Qrs 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 2022-12-14.

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.