FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Non-Allograft Tissue
PMA: P170006
·
Supplement: S013
·
Decision Jul 29, 2019
Classifications
1
FEI Numbers
19
Registration Numbers
19
Basic Information
- Device Name
- Heart-Valve, Non-Allograft Tissue
- Trade Name
- Avalus Bioprosthesis
- PMA Number
- P170006
- Supplement Number
- S013
- 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
- July 29, 2019
- Date Received
- May 9, 2019
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for changes to the liquid chemical sterilization cycle parameters for the Avalus Bioprosthesis.
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 |