FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Auditory Brainstem
PMA: P000015
·
Supplement: S041
·
Decision Jul 2, 2020
Classifications
1
FEI Numbers
10
Registration Numbers
10
Basic Information
- Device Name
- Implant, Auditory Brainstem
- Trade Name
- Nucleus Auditory Brainstem Implant
- PMA Number
- P000015
- Supplement Number
- S041
- Device Class
- FDA Class 3
- Product Code
- MHE
- Generic Name
- Implant, auditory brainstem
- Medical Specialty
- Unknown
- Advisory Committee
- Ear, Nose, Throat
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- July 2, 2020
- Date Received
- November 13, 2019
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for the Kanso 2 Sound Processor and associated accessories, Nucleus 7 for Nucleus 22, SmartNav System including SmartNav App and CP1150S Surgical Processor, and Custom Sound Pro.
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 |
|---|---|---|---|
| MHE | Implant, Auditory Brainstem | FDA class 3 | Unknown |