FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Implant, Cochlear
PMA: P000025
·
Supplement: S083
·
Decision Dec 29, 2015
Classifications
1
FEI Numbers
22
Registration Numbers
22
Basic Information
- Device Name
- Implant, Cochlear
- Trade Name
- COMBI 40+ COCHLEAR IMPLANT SYSTEM (MAESTRO COCHLEAR IMPLANT SYSTEM)
- PMA Number
- P000025
- Supplement Number
- S083
- 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
- December 29, 2015
- Date Received
- November 30, 2015
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
ALTERNATIVES TO BATCH TESTING FOR BACTERIAL ENDOTOXINS AND ESTABLISHMENT OF A DYNAMIC SAMPLING PLAN.
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 |