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

Implant, Cochlear

PMA: P970051 · Supplement: S232 · Decision Nov 13, 2024
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
Nucleus CI632 Cochlear Implant, Nucleus CI532 Cochlear Implant
PMA Number
P970051
Supplement Number
S232
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
November 13, 2024
Date Received
October 17, 2024
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

for addition of a new cleanroom at the Lane Cove manufacturing site

Classifications

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

Product Code Device Name
MCM Implant, Cochlear