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HexaFlow™ Irrigation Pumo AFR-00004, HexaGen TM RF Generator AFR-00005, HexaPulse TM PF Generator AFR-00008

FDA premarket approval P240013/S014 · decided 2025-07-23

Approval details

PMA number
P240013
Supplement
S014
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
HexaFlow™ Irrigation Pumo AFR-00004, HexaGen TM RF Generator AFR-00005, HexaPulse TM PF Generator AFR-00008
Generic name
Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation
Applicant
Medtronic, Inc.
Date received
2025-06-26
Decision date
2025-07-23
Days to decision
27 days
Decision code
OK30
Product code
QZI
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
the addition of new manufacturing tool (pump emulator) and associated manufacturing process at Medtronic Billerica manufacturing facility (Billerica, MA)

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