FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Cochlear
PMA: P000025
·
Supplement: S068
·
Decision May 16, 2013
Classifications
1
FEI Numbers
22
Registration Numbers
22
Basic Information
- Device Name
- Implant, Cochlear
- Trade Name
- MED-EL COMBI 40+ COHLEAR IMPLANT SYSTEM
- PMA Number
- P000025
- Supplement Number
- S068
- 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
- May 16, 2013
- Date Received
- March 1, 2013
- Supplement Type
- Real-Time Process
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE REUSABLE MI1000 PIN DRILL GUIDE WHICH ASSISTS IN THE SURGICAL IMPLANTATION OF THE APPROVED MI1000 CONCERT PIN IMPLANT.
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 |