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WHITER BITER CROWN

K913152 Class I Traditional
Decision Date
1991-09-30
Sponsor / Applicant
George M. Wilson, Dds

Technical Specification

510(k) Submission ID K913152
Product Code ELZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3330
Decision Date 1991-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WHITER BITER CROWN received FDA 510(k) clearance under submission number K913152, sponsored by George M. Wilson, Dds. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-09-30.

Classification & Regulation

This clearance is catalogued under FDA product code ELZ and 21 CFR 872.3330, within the Dental review panel as a Class I device.