meddevicedb.com FDA Device Reference

TALLADIUM TILITE CERAMIC ALLOY

K894085 Class II Traditional
Decision Date
1989-12-20
Sponsor / Applicant
Talladium, Inc.

Technical Specification

510(k) Submission ID K894085
Product Code EJH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3710
Decision Date 1989-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TALLADIUM TILITE CERAMIC ALLOY received FDA 510(k) clearance under submission number K894085, sponsored by Talladium, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code EJH and 21 CFR 872.3710, within the Dental review panel as a Class II device.