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 | Device Class | Medical Specialty |
|---|---|---|---|
| MCM | Implant, Cochlear | FDA class 3 | Unknown |