Cordella Pulmonary Artery Sensor System (CorPASS)
FDA premarket approval P230040/S021 · decided 2025-09-29
Approval details
- PMA number
- P230040
- Supplement
- S021
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Cordella Pulmonary Artery Sensor System (CorPASS)
- Generic name
- System, hemodynamic, implantable
- Applicant
- Endotronix, Inc.
- Date received
- 2025-09-05
- Decision date
- 2025-09-29
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- MOM
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Naperville, IL
- Statement
- implement a change in the incoming inspection sampling plan for a device component
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