FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implant, Cochlear

PMA: P000025 · Supplement: S108 · Decision May 8, 2019
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
FineTuner Echo
PMA Number
P000025
Supplement Number
S108
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
May 8, 2019
Date Received
January 31, 2019
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the FineTuner Echo of the Med-El Cochlear Implant System, which is a remote control (optional accessory) for compatible audio processors. It is the hardware successor of the previously approved FineTuner and includes minor design changes to the graphical user interface.

Classifications

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

Product Code Device Name
MCM Implant, Cochlear