FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Cochlear
PMA: P890027
·
Supplement: S056
·
Decision Oct 16, 2007
Classifications
1
FEI Numbers
22
Registration Numbers
22
Basic Information
- Device Name
- Implant, Cochlear
- Trade Name
- NUCLEUS 22 COCHLEAR IMPLANT SYSTEM
- PMA Number
- P890027
- Supplement Number
- S056
- Device Class
- FDA Class 3
- Product Code
- MCM
- Generic Name
- Implant, cochlear
- Medical Specialty
- Unknown
- Advisory Committee
- Ear, Nose, Throat
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- October 16, 2007
- Date Received
- September 14, 2007
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR MODIFICATIONS TO CUSTOM SOUND PROGRAMMING SOFTWARE TO PROVIDE RECEIPTS OF PREVIOUS GENERATION NUCLEUS 22 COCHLEAR IMPLANTS WITH ACCESS TO THE NUCLEUS FREEDOM SPEECH PROCESSOR.
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 |