FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Mechanical
PMA: P990046
·
Supplement: S032
·
Decision Jun 7, 2013
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Heart-Valve, Mechanical
- Trade Name
- OPEN PIVOT HEART VALVE
- PMA Number
- P990046
- Supplement Number
- S032
- Device Class
- FDA Class 3
- Product Code
- LWQ
- Generic Name
- HEART-VALVE, MECHANICAL
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 7, 2013
- Date Received
- March 28, 2013
- 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 IN MINNEAPOLIS,MINNESOTA.
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 |
|---|---|---|---|
| LWQ | Heart-Valve, Mechanical | FDA class 3 | Unknown |