510(k) K112053

OBC BONE ANCHORED HEARING SYSTEM by Oticon Medical AB — Product Code MAH

K112053 is an FDA 510(k) premarket notification submitted by Oticon Medical AB for the device "OBC BONE ANCHORED HEARING SYSTEM". The FDA issued a decision of Substantially Equivalent on November 18, 2011. The device falls under product code MAH (Hearing Aid, Bone Conduction, Implanted), a Class II device regulated under 21 CFR 874.3302. Oticon Medical AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 18, 2011
Date Received
July 19, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hearing Aid, Bone Conduction, Implanted
Device Class
Class II
Regulation Number
874.3302
Review Panel
EN
Submission Type