meddevicedb.com FDA Device Reference

Exceed Tx

K150702 Class II Traditional
Decision Date
2016-03-24
Sponsor / Applicant
Great Lakes Orthodontics, Ltd.

Technical Specification

510(k) Submission ID K150702
Product Code DYW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2016-03-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Exceed Tx received FDA 510(k) clearance under submission number K150702, sponsored by Great Lakes Orthodontics, 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 2016-03-24.

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.