FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation
PMA: P200035
·
Supplement: S006
·
Decision Aug 8, 2023
Classifications
1
FEI Numbers
6
Registration Numbers
6
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
- S006
- 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
- August 8, 2023
- Date Received
- December 21, 2022
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Approval for a manufacturing site located at Integrated Technologies Ltd, Viking House, Ellingham Way, Ashford, Kent, TN23 6NF, UK.
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 |