510(k) K152820

Ponto Bone Anchored Hearing System by Oticon Medical AB — Product Code MAH

K152820 is an FDA 510(k) premarket notification submitted by Oticon Medical AB for the device "Ponto Bone Anchored Hearing System". The FDA issued a decision of Substantially Equivalent on January 22, 2016. 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
January 22, 2016
Date Received
September 28, 2015
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