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OBC BONE ANCHORED HEARING SYSTEM

K112053 Class II Traditional
Decision Date
2011-11-18
Sponsor / Applicant
Oticon Medical AB

Technical Specification

510(k) Submission ID K112053
Product Code MAH
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3302
Decision Date 2011-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OBC BONE ANCHORED HEARING SYSTEM received FDA 510(k) clearance under submission number K112053, sponsored by Oticon Medical AB. 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 2011-11-18.

Classification & Regulation

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