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ANTERIORS AND POSTERIORS, PLASTIC

K780217 Class II Traditional
Decision Date
1978-03-15
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K780217
Product Code ELM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3590
Decision Date 1978-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANTERIORS AND POSTERIORS, PLASTIC received FDA 510(k) clearance under submission number K780217, 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 1978-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code ELM and 21 CFR 872.3590, within the Dental review panel as a Class II device.