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