FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Implant, Cochlear

PMA: P970051 · Supplement: S155 · Decision Jan 19, 2017
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
NUCLEUS COCHLEAR IMPLANT SYSTEM
PMA Number
P970051
Supplement Number
S155
Device Class
FDA Class 3
Product Code
MCM
Generic Name
Implant, cochlear
Medical Specialty
Unknown
Advisory Committee
Ear, Nose, Throat
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
January 19, 2017
Date Received
December 21, 2016
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Addition of an alternative PCB supplier for the CP900 Sound Processor. This update will add AT&S, an already approved Cochlear vendor, as an addition to the existing CP900 Sound Processor PCB supplier, GS Swiss

Classifications

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

Product Code Device Name
MCM Implant, Cochlear