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BILATERAL FITTING OF THE BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM.

K011438 Class II Traditional
Decision Date
2001-07-23
Sponsor / Applicant
Entific Medical Systems, Inc.

Technical Specification

510(k) Submission ID K011438
Product Code LXB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3302
Decision Date 2001-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BILATERAL FITTING OF THE BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM. received FDA 510(k) clearance under submission number K011438, sponsored by Entific Medical Systems, 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 2001-07-23.

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.