FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Non-Allograft Tissue
PMA: P970031
·
Supplement: S078
·
Decision Feb 12, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Heart-Valve, Non-Allograft Tissue
- Trade Name
- Freestyle Bioprosthesis
- PMA Number
- P970031
- Supplement Number
- S078
- 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
- February 12, 2026
- Date Received
- September 29, 2025
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
approval for a Pre-Determined Change Control Plan (PCCP) that establishes a standardized qualification process for new bovine and porcine tissue suppliers, provided they do not impact the tissue's specifications, the established methods for its sourcing, handling, and testing, or the qualification standards for supplier facilities and personnel for the devices under the above PMAs
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 |