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AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE

K040547 Class II Traditional
Decision Date
2004-03-19
Sponsor / Applicant
Harry J. Bosworth Co.

Technical Specification

510(k) Submission ID K040547
Product Code DYH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3750
Decision Date 2004-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE received FDA 510(k) clearance under submission number K040547, sponsored by Harry J. Bosworth Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.