Atlas FDA

ARCTIC FRONT CARDIAC CRYOABLATION CATHETER, ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER, ARCTIC FRONT ST CARDIAC

FDA premarket approval P100010/S056 · decided 2016-07-29

Approval details

PMA number
P100010
Supplement
S056
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ARCTIC FRONT CARDIAC CRYOABLATION CATHETER, ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER, ARCTIC FRONT ST CARDIAC
Generic name
Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
Applicant
Medtronic Cryocath, LP
Date received
2016-06-07
Decision date
2016-07-29
Days to decision
52 days
Decision code
APPR
Product code
OAE
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for modification to the display monitor of the Gen V Universal CryoConsole (model 106A3).

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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