meddevicedb.com FDA Device Reference

HOWMEDICA A-30 DENTAL ALLOY

K791304 Class II Traditional
Decision Date
1979-10-04
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K791304
Product Code EJT
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 1979-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOWMEDICA A-30 DENTAL ALLOY received FDA 510(k) clearance under submission number K791304, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1979-10-04.

Classification & Regulation

This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.