meddevicedb.com FDA Device Reference

STERNGOLD BIO-5 (1127210)

K962326 Class II Traditional
Decision Date
1996-07-24
Sponsor / Applicant
Sterngold/Implamed

Technical Specification

510(k) Submission ID K962326
Product Code EJT
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 1996-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERNGOLD BIO-5 (1127210) received FDA 510(k) clearance under submission number K962326, sponsored by Sterngold/Implamed. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1996-07-24.

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.