meddevicedb.com FDA Device Reference

PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM

K061252 Class II Traditional
Decision Date
2007-02-12
Sponsor / Applicant
Primus Consulting

Technical Specification

510(k) Submission ID K061252
Product Code DYH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3750
Decision Date 2007-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM received FDA 510(k) clearance under submission number K061252, sponsored by Primus Consulting. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.