PMA
P200035: OrganOx metra System
FDA PMA · Normothermic machine perfusion system for the preservation of donor livers prior to transplantation · Organox Limited
Key facts
| PMA number | P200035 |
|---|---|
| Trade name | OrganOx metra System |
| Generic name | Normothermic machine perfusion system for the preservation of donor livers prior to transplantation |
| Applicant | Organox Limited |
| Owner/operator | OrganOx Limited |
| Product code | QQK |
| Approval date | Dec 9, 2021 |
| Docket number | 21M-1317 |
| Notice date | Dec 17, 2021 |
| Establishment registration | 3011560054 |
| FEI number | 3011560054 |
At a glance
- 10–99 Supplements
- Oct 9, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 1–9 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: