meddevicedb.com FDA Device Reference

STERN ERA ALIGNMENT CORRECTION IMPLANT ABUTMENT

K921010 Class II Traditional
Decision Date
1992-09-01
Sponsor / Applicant
Apm Stern Gold

Technical Specification

510(k) Submission ID K921010
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1992-09-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERN ERA ALIGNMENT CORRECTION IMPLANT ABUTMENT received FDA 510(k) clearance under submission number K921010, sponsored by Apm Stern Gold. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-09-01.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.