FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Implant, Hearing, Active, Middle Ear, Partially Implanted
PMA: P990052
·
Supplement: S012
·
Decision Oct 13, 2006
Classifications
1
FEI Numbers
4
Registration Numbers
4
Basic Information
- Device Name
- Implant, Hearing, Active, Middle Ear, Partially Implanted
- Trade Name
- VIBRANT SOUNDBRIDGE MIDDLE EAR IMPLANT SYSTEM
- PMA Number
- P990052
- Supplement Number
- S012
- Device Class
- FDA Class 3
- Product Code
- MPV
- Generic Name
- Implant, hearing, active, middle ear, partially implanted
- Medical Specialty
- Unknown
- Advisory Committee
- Ear, Nose, Throat
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- October 13, 2006
- Date Received
- December 1, 2005
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT MED-EL ELEKTROMEDIZINISCHE GERATE (CONTRACT MANUFACTURER FOR VIBRANT MED-EL) GMBH OF INNSBRUCK, AUSTRIA, FOR THE LASER WELDING OF THE PRE WELDED DEMODULATOR UNIT AND THE BOBBIN.
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 |
|---|---|---|---|
| MPV | Implant, Hearing, Active, Middle Ear, Partially Implanted | FDA class 3 | Unknown |