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

Implant, Cochlear

PMA: P970051 · Supplement: S136 · Decision Nov 20, 2015
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Implant, Cochlear
Trade Name
NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
PMA Number
P970051
Supplement Number
S136
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 20, 2015
Date Received
October 23, 2015
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

THE INTRODUCTION OF AN ADDITIONAL CLEANING STEP TO REMOVE PRIMER RESIDUE PRIOR TO CURING FROM THE WELD SURFACE OF THE NUCLEUS CI 500 SERIES IMPLANTS (NUCLEUS CI512 AND 522).

Classifications

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

Product Code Device Name
MCM Implant, Cochlear