OrganOx metra® System
FDA premarket approval P200035/S004 · decided 2024-08-22
Approval details
- PMA number
- P200035
- Supplement
- S004
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- OrganOx metra® System
- Generic name
- Normothermic machine perfusion system for the preservation of donor livers prior to transplantation
- Applicant
- Organox Limited
- Date received
- 2022-06-17
- Decision date
- 2024-08-22
- Days to decision
- 797 days
- Decision code
- APPR
- Product code
- QQK
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Oxford
- Statement
- response to the additional information in the Not Approvable letter sent from FDA on January 18, 2024 for the cleaning validation of the MLA using quantitative test methods.
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