Atlas FDA

CorPASS System

FDA premarket approval P230040/S024 · decided 2025-11-25

Approval details

PMA number
P230040
Supplement
S024
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CorPASS System
Generic name
System, hemodynamic, implantable
Applicant
Endotronix, Inc.
Date received
2025-10-14
Decision date
2025-11-25
Days to decision
42 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 implant sensor printed circuit board

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