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HexaGen™ RF Generator, HexaPulse™ PF Generator, HexaFlow™ Irrigation Pump

FDA premarket approval P240013/S013 · decided 2025-08-15

Approval details

PMA number
P240013
Supplement
S013
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
HexaGen™ RF Generator, HexaPulse™ PF Generator, HexaFlow™ Irrigation Pump
Generic name
Percutaneous Cardiac Ablation Catheter for Treatment of Atrial Fibrillation with Irreversible Electroporation
Applicant
Medtronic, Inc.
Date received
2025-06-25
Decision date
2025-08-15
Days to decision
51 days
Decision code
APPR
Product code
QZI
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
approval for a manufacturing site located at Plexus Inc., 2400 Millbrook Dr., Buffalo Grove, IL 60089 (FEI: 3004105270)

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510(k) clearances by this applicant

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