meddevicedb.com FDA Device Reference

HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES

K001406 Class II Traditional
Decision Date
2000-08-08
Sponsor / Applicant
Mednet Locator, Inc.

Technical Specification

510(k) Submission ID K001406
Product Code ETA
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3495
Decision Date 2000-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES received FDA 510(k) clearance under submission number K001406, sponsored by Mednet Locator, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2000-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code ETA and 21 CFR 874.3495, within the Ear, Nose, Throat review panel as a Class II device.