FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Cochlear

PMA: P960058 · Supplement: S139 · Decision Jul 18, 2019
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
HiResolution Bionic Ear System
PMA Number
P960058
Supplement Number
S139
Device Class
FDA Class 3
Product Code
MCM
Generic Name
Implant, cochlear
Medical Specialty
Unknown
Advisory Committee
Ear, Nose, Throat
Decision
Approved
Decision Code
APPR
Decision Date
July 18, 2019
Date Received
May 6, 2019
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for a new headpiece variant, the UHP 3D Plus and associated magnets, 3D Magnet Max and 3D Magnet Plus.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MCM Implant, Cochlear