FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation
PMA: P200035
·
Supplement: S001
·
Decision Apr 12, 2022
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
- S001
- 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
- April 12, 2022
- Date Received
- March 15, 2022
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the revised protocol for the post-approval study (PAS) protocol.
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 |