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GOTHIC ARCH TRACING

K771176 Class I Traditional
Decision Date
1977-08-16
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K771176
Product Code KZO
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3150
Decision Date 1977-08-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GOTHIC ARCH TRACING received FDA 510(k) clearance under submission number K771176, sponsored by Dentsply Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1977-08-16.

Classification & Regulation

This clearance is catalogued under FDA product code KZO and 21 CFR 872.3150, within the Dental review panel as a Class I device.