meddevicedb.com FDA Device Reference

ORTHODONTIC PLASTIC BRACKET

K891372 Class II Traditional
Decision Date
1989-03-31
Sponsor / Applicant
American Orthodontics

Technical Specification

510(k) Submission ID K891372
Product Code DYW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 1989-03-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHODONTIC PLASTIC BRACKET received FDA 510(k) clearance under submission number K891372, sponsored by American Orthodontics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-03-31.

Classification & Regulation

This clearance is catalogued under FDA product code DYW and 21 CFR 872.5470, within the Dental review panel as a Class II device.