meddevicedb.com FDA Device Reference

NOBELPHARMA BONE ANCHORED HEARING AID

K955713 Class II Traditional
Decision Date
1996-08-09
Sponsor / Applicant
Nobelpharma USA, Inc.

Technical Specification

510(k) Submission ID K955713
Product Code LXB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3302
Decision Date 1996-08-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOBELPHARMA BONE ANCHORED HEARING AID received FDA 510(k) clearance under submission number K955713, sponsored by Nobelpharma USA, 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 1996-08-09.

Classification & Regulation

This clearance is catalogued under FDA product code LXB and 21 CFR 874.3302, within the Ear, Nose, Throat review panel as a Class II device.