FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
System, Hemodynamic, Implantable
PMA: P230040
·
Supplement: S025
·
Decision Jan 9, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- System, Hemodynamic, Implantable
- Trade Name
- Cordella Pulmonary Artery Sensor System (CorPASS)
- PMA Number
- P230040
- Supplement Number
- S025
- Device Class
- FDA Class 3
- Product Code
- MOM
- Generic Name
- System, hemodynamic, implantable
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- January 9, 2026
- Date Received
- December 15, 2025
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
implement a manufacturing process change at the supplier.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MOM | System, Hemodynamic, Implantable | FDA class 3 | Unknown |