FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Non-Allograft Tissue
PMA: P150048
·
Supplement: S047
·
Decision Mar 16, 2022
Classifications
1
FEI Numbers
19
Registration Numbers
19
Basic Information
- Device Name
- Heart-Valve, Non-Allograft Tissue
- Trade Name
- MITRIS RESILIA Mitral Valve
- PMA Number
- P150048
- Supplement Number
- S047
- 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
- March 16, 2022
- Date Received
- August 3, 2020
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for material and design modifications related to the wireform, sewing ring, valve holder and valve handle
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 |