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PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION

K081291 Class II Special
Decision Date
2008-05-22
Sponsor / Applicant
Dentsply Interntional

Technical Specification

510(k) Submission ID K081291
Product Code DYH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3750
Decision Date 2008-05-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION received FDA 510(k) clearance under submission number K081291, sponsored by Dentsply Interntional. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-05-22.

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.