FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Non-Allograft Tissue
PMA: P060038
·
Supplement: S024
·
Decision Nov 24, 2015
Classifications
1
FEI Numbers
19
Registration Numbers
19
Basic Information
- Device Name
- Heart-Valve, Non-Allograft Tissue
- Trade Name
- MITROFLOW AORTIC PERICARDIAL HEART VALVE (MAPHV)
- PMA Number
- P060038
- Supplement Number
- S024
- Device Class
- FDA Class 3
- Product Code
- LWR
- Generic Name
- heart-valve, non-allograft tissue
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- November 24, 2015
- Date Received
- September 22, 2015
- Supplement Type
- Real-Time Process
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR REVISIONS TO THE MRI SAFETY LABELING.
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 |
|---|---|---|---|
| LWR | Heart-Valve, Non-Allograft Tissue | FDA class 3 | Unknown |