FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Heart-Valve, Non-Allograft Tissue
PMA: P970031
·
Supplement: S070
·
Decision Aug 10, 2023
Classifications
1
FEI Numbers
19
Registration Numbers
19
Basic Information
- Device Name
- Heart-Valve, Non-Allograft Tissue
- Trade Name
- Hancock II Bioprosthesis
- PMA Number
- P970031
- Supplement Number
- S070
- Device Class
- FDA Class 3
- Product Code
- LWR
- Generic Name
- heart-valve, non-allograft tissue
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- August 10, 2023
- Date Received
- July 31, 2023
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Manufacturing site addition for the supplier of the primary packaging component for the Mosaic, Freestyle, Hancock II, and Avalus bioprostheses.
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 |