Cordella Pulmonary Artery Sensor System (CorPASS)
FDA premarket approval P230040/S002 · decided 2024-08-22
Approval details
- PMA number
- P230040
- Supplement
- S002
- 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
- 2024-07-24
- Decision date
- 2024-08-22
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- MOM
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Naperville, IL
- Statement
- the addition of an alternative supplier for the sensor printed circuit boards
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