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ACRYLIC HERBST APPLIANCE

K111009 Class II Traditional
Decision Date
2011-07-22
Sponsor / Applicant
Embassy Dental Laboratory

Technical Specification

510(k) Submission ID K111009
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2011-07-22
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 K111009, sponsored by Embassy Dental Laboratory. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2011-07-22.

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.