Atlas FDA

Nitron CryoConsole, Nitron Foot Switch

FDA premarket approval P020045/S110 · decided 2024-11-25

Approval details

PMA number
P020045
Supplement
S110
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Nitron CryoConsole, Nitron Foot Switch
Generic name
Cardiac ablation percutaneous catheter
Applicant
Medtronic Cryocath, LP
Date received
2024-08-30
Decision date
2024-11-25
Days to decision
87 days
Decision code
APPR
Product code
LPB
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
approval for a Nitron CryoConsole software upgrade from version 1.0 to version 1.1 and a new optional accessory called the Nitron Foot Switch

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510(k) clearances by this applicant

RecordFirmDate
FlexCath Advance Steerable Sheath and Dilator (K202620)Medtronic Cryocath, LP2020-11-13
FlexCath Advance Steerable Sheath and Dilator (K183174)Medtronic Cryocath, LP2018-11-26
FlexCath Select Steerable Shealth and Dilator (K163268)Medtronic Cryocath, LP2017-02-02
FlexCath Select Steerable Sheath (10 French) (K142684)Medtronic Cryocath, LP2014-11-06
FLEXCATH ADVANCE STEERABLE SHEATH (12 FRENCH) (K123591)Medtronic Cryocath, LP2012-12-27
FLEXCATH STEERABLE SHEATH (12 FRENCH), FLEXCATH STEERABLE SHEATH (10 FRENCH) MODEL 3FC12, 3FC10 (K102176)Medtronic Cryocath, LP2010-09-01