meddevicedb.com FDA Device Reference

MTM CLEAR ALIGNER IN-OFFICE

K123925 Class II Traditional
Decision Date
2013-05-24
Sponsor / Applicant
Dentsply International, Inc.

Technical Specification

510(k) Submission ID K123925
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2013-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTM CLEAR ALIGNER IN-OFFICE received FDA 510(k) clearance under submission number K123925, sponsored by Dentsply International, 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 2013-05-24.

Classification & Regulation

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