FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation
PMA: P200035
·
Supplement: S032
·
Decision Mar 16, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
Basic Information
- Device Name
- Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation
- Trade Name
- OrganOx metra® System
- PMA Number
- P200035
- Supplement Number
- S032
- Device Class
- FDA Class 3
- Product Code
- QQK
- Generic Name
- Normothermic machine perfusion system for the preservation of donor livers prior to transplantation
- Medical Specialty
- Unknown
- Advisory Committee
- Gastroenterology, Urology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 16, 2026
- Date Received
- December 19, 2025
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
modification of the battery pack fixture that secures the two rechargeable batteries within the base of the metra® System
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 |
|---|---|---|---|
| QQK | Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation | FDA class 3 | Unknown |