meddevicedb.com FDA Device Reference

CompleClear Plastic Orthodontic Bracket and Wire Appliance

K150830 Class II Traditional
Decision Date
2016-08-26
Sponsor / Applicant
Oracrew

Technical Specification

510(k) Submission ID K150830
Product Code DYW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2016-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CompleClear Plastic Orthodontic Bracket and Wire Appliance received FDA 510(k) clearance under submission number K150830, sponsored by Oracrew. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-08-26.

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.