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BRUXZIR SHADED

K130924 Class II Special
Decision Date
2013-05-16
Sponsor / Applicant
Prismatik Dentalcraft, Inc.

Technical Specification

510(k) Submission ID K130924
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2013-05-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRUXZIR SHADED received FDA 510(k) clearance under submission number K130924, sponsored by Prismatik Dentalcraft, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.