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ACRYLIC HERBST APPLIANCE

K113126 Class II Traditional
Decision Date
2013-07-17
Sponsor / Applicant
Gergens Orthodontic Lab

Technical Specification

510(k) Submission ID K113126
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2013-07-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACRYLIC HERBST APPLIANCE received FDA 510(k) clearance under submission number K113126, sponsored by Gergens Orthodontic Lab. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-07-17.

Classification & Regulation

This clearance is catalogued under FDA product code LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.