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
QQK Normothermic Machine Perfusion System For The Preservation Of Donor Livers Prior To Transplantation