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STERN ERA IMPLANT ABUTMENT

K914764 Class II Traditional
Decision Date
1992-01-17
Sponsor / Applicant
Sterngold/Implamed

Technical Specification

510(k) Submission ID K914764
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1992-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERN ERA IMPLANT ABUTMENT received FDA 510(k) clearance under submission number K914764, 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 1992-01-17.

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.