THERAPY COOL PATH DUO/ SAFIRE BLU DUO ABLATION CATHETER AND IBI 1500T9-CP V1.6 CARDIAC ABLATION GENERATOR

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Premarket Approval P110016

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

Approval for the therapy cool path duo ablation catheter; safire blu duo ablation catheter; and ibi 1500t-9 vi. 6 cardiac ablation generator. This device is indicated for use with the compatible irrigation pumpand 1500t9-cp radiofrequency (rf) generator at a maximum of 50 watts. The catheter is intended for creating endocardial lesions during cardiac ablation procedures (mapping, stimulation and ablation) for the treatment of typical atrial flutter.

DeviceTHERAPY COOL PATH DUO/ SAFIRE BLU DUO ABLATION CATHETER AND IBI 1500T9-CP V1.6 CARDIAC ABLATION GENERATOR
Classification NameCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
Generic NameCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
ApplicantSt. Jude Medical, Inc. (Irvine Biomedical)
Date Received2011-04-15
Decision Date2012-01-25
Notice Date2012-02-02
PMAP110016
SupplementS
Product CodeOAD
Docket Number12M-0112
Advisory CommitteeCardiovascular
Expedited ReviewNo
Combination Product No
Applicant Address St. Jude Medical, Inc. (Irvine Biomedical) 2375 Morse Avenue irvine, CA 92614-6233
Summary:Summary of Safety and Effectiveness
Labeling: Labeling
Approval Order: Approval Order

Supplemental Filings

Supplement NumberDateSupplement Type
P110016Original Filing
S081 2022-11-14 30-day Notice
S080
S079 2021-09-14 30-day Notice
S078 2021-08-24 30-day Notice
S077 2021-05-26 30-day Notice
S076 2021-04-19 30-day Notice
S075 2021-04-13 30-day Notice
S074 2021-02-25 30-day Notice
S073 2021-01-13 Real-time Process
S072 2020-10-28 Real-time Process
S071 2020-09-18 30-day Notice
S070
S069 2020-05-06 30-day Notice
S068 2020-03-19 30-day Notice
S067
S066 2020-02-04 30-day Notice
S065 2019-09-26 30-day Notice
S064 2019-09-12 Special (immediate Track)
S063 2019-06-24 Normal 180 Day Track No User Fee
S062 2019-04-26 30-day Notice
S061 2019-03-25 30-day Notice
S060 2019-03-15 30-day Notice
S059 2019-02-14 Normal 180 Day Track No User Fee
S058 2018-12-12 Special (immediate Track)
S057 2018-05-18 Special (immediate Track)
S056 2018-03-27 30-day Notice
S055 2018-02-14 30-day Notice
S054 2018-02-12 30-day Notice
S053 2018-02-05 30-day Notice
S052 2017-11-28 30-day Notice
S051 2017-11-02 30-day Notice
S050 2017-10-27 135 Review Track For 30-day Notice
S049 2017-08-22 30-day Notice
S048
S047 2017-06-30 30-day Notice
S046 2017-05-04 30-day Notice
S045 2017-04-28 30-day Notice
S044 2017-05-01 30-day Notice
S043 2017-04-28 30-day Notice
S042
S041 2017-03-28 30-day Notice
S040 2017-03-20 30-day Notice
S039 2017-03-13 30-day Notice
S038 2017-03-03 30-day Notice
S037
S036 2016-09-08 Special (immediate Track)
S035 2016-08-12 30-day Notice
S034 2016-06-24 135 Review Track For 30-day Notice
S033 2016-05-27 30-day Notice
S032 2016-05-27 30-day Notice
S031 2016-03-17 30-day Notice
S030 2016-03-14 30-day Notice
S029 2016-02-19 30-day Notice
S028 2015-11-25 30-day Notice
S027 2015-11-20 Real-time Process
S026 2015-11-12 Special (immediate Track)
S025 2015-11-05 Normal 180 Day Track
S024 2015-10-30 Normal 180 Day Track No User Fee
S023 2015-09-23 30-day Notice
S022 2015-09-01 30-day Notice
S021 2015-08-21 Normal 180 Day Track No User Fee
S020 2015-08-20 30-day Notice
S019
S018 2015-06-29 Special (immediate Track)
S017 2015-04-20 30-day Notice
S016 2015-02-05 Normal 180 Day Track No User Fee
S015 2015-02-04 Special (immediate Track)
S014 2014-11-07 Real-time Process
S013 2014-06-19 Normal 180 Day Track
S012 2014-04-30 Normal 180 Day Track No User Fee
S011 2014-03-03 Real-time Process
S010 2013-11-27 Normal 180 Day Track
S009 2013-08-30 30-day Notice
S008 2013-04-01 Panel Track
S007 2013-03-07 Normal 180 Day Track
S006 2013-01-24 Real-time Process
S005 2012-07-11 135 Review Track For 30-day Notice
S004 2012-07-10 Real-time Process
S003 2012-06-25 Normal 180 Day Track
S002 2012-05-11 Real-time Process
S001 2012-03-29 135 Review Track For 30-day Notice

NIH GUDID Devices

Device IDPMASupp
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05415067024916 P110016 025

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