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Carriere Motion Clear Class II

K160720 Class II Traditional
Decision Date
2016-11-28
Sponsor / Applicant
Ortho Organizers, Inc.

Technical Specification

510(k) Submission ID K160720
Product Code DYW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2016-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Carriere Motion Clear Class II received FDA 510(k) clearance under submission number K160720, sponsored by Ortho Organizers, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-11-28.

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.