This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Approval for the valiant thoracic stent graft with captivia delivery system (valiant captivia). This device is indicated for the endovascular repair of all lesions of the descending thoracic aorta (dta) in patients having the appropriate anatomy including: 1) iliac or femoral artery access vessel morphology that is compatible with vascular access techniques, devices or accessories; nonaneurysmal aortic diameter in the range of 18 mm to 42 mm (fusiform and saccular aneurysms/penetrating ulcers), or 18 mm to 44 mm (blunt traumatic aortic injuries), or 20 mm to 44 mm (dissections); and nonaneurysmal aortic proximal and distal neck lengths ¿ 20 (fusiform and saccular aneurysms/ penetrating ulcers), landing zone ¿20 mm proximal to the primary entry tear (blunt traumatic aortic injuries, dissections). The proximal extent of the landing zone must not be dissected.
Device | VALIANT THORACIC STENT GRAFT WITH CAPTIVIA DELIVERY SYSTEM |
Classification Name | System, Endovascular Graft, Aortic Aneurysm Treatment |
Generic Name | System, Endovascular Graft, Aortic Aneurysm Treatment |
Applicant | Medtronic Vascular |
Date Received | 2013-07-29 |
Decision Date | 2014-01-22 |
Notice Date | 2014-02-04 |
PMA | P100040 |
Supplement | S012 |
Product Code | MIH |
Docket Number | 14M-167 |
Advisory Committee | Cardiovascular |
Supplement Type | Panel Track |
Supplement Reason | Labeling Change - Indications/instructions/shelf Life/tradename |
Expedited Review | No |
Combination Product | No |
Applicant Address | Medtronic Vascular 3576 Unocal Place santa Rosa, CA 95403 |
Summary: | Summary of Safety and Effectiveness |
Labeling: | Labeling |
Post-Approval Study: | Show Report Schedule and Study Progress |
Approval Order: | Approval Order |
Supplement Number | Date | Supplement Type |
---|---|---|
P100040 | Original Filing | |
S055 | 2022-11-29 | 30-day Notice |
S054 | 2022-11-18 | 30-day Notice |
S053 | 2022-10-31 | 30-day Notice |
S052 | 2022-09-27 | 30-day Notice |
S051 | 2022-03-23 | 30-day Notice |
S050 | 2021-11-30 | 30-day Notice |
S049 | ||
S048 | 2021-07-27 | 30-day Notice |
S047 | 2021-04-23 | Special (immediate Track) |
S046 | 2021-03-17 | 30-day Notice |
S045 | 2021-03-04 | 30-day Notice |
S044 | 2021-02-25 | 30-day Notice |
S043 | ||
S042 | ||
S041 | 2020-09-04 | Normal 180 Day Track No User Fee |
S040 | 2020-07-14 | 30-day Notice |
S039 | 2019-09-17 | 30-day Notice |
S038 | 2019-04-05 | 30-day Notice |
S037 | 2018-09-24 | 30-day Notice |
S036 | 2018-04-23 | Panel Track |
S035 | 2018-04-05 | 30-day Notice |
S034 | 2018-01-03 | 30-day Notice |
S033 | 2017-11-20 | 30-day Notice |
S032 | 2017-07-14 | 30-day Notice |
S031 | 2017-04-19 | 30-day Notice |
S030 | ||
S029 | 2017-01-12 | 30-day Notice |
S028 | 2016-08-17 | 135 Review Track For 30-day Notice |
S027 | 2016-07-13 | 30-day Notice |
S026 | 2016-06-29 | 30-day Notice |
S025 | 2015-08-31 | 135 Review Track For 30-day Notice |
S024 | 2015-08-07 | 30-day Notice |
S023 | 2015-07-31 | 30-day Notice |
S022 | 2015-05-26 | 30-day Notice |
S021 | 2015-05-20 | Normal 180 Day Track No User Fee |
S020 | 2015-03-20 | 135 Review Track For 30-day Notice |
S019 | 2014-04-11 | 30-day Notice |
S018 | ||
S017 | 2014-02-07 | Real-time Process |
S016 | 2014-01-31 | 30-day Notice |
S015 | 2013-12-16 | 30-day Notice |
S014 | 2013-11-15 | 30-day Notice |
S013 | 2013-11-04 | Real-time Process |
S012 | 2013-07-29 | Panel Track |
S011 | 2013-04-04 | 30-day Notice |
S010 | 2013-01-29 | 30-day Notice |
S009 | 2012-08-24 | 30-day Notice |
S008 | 2012-04-30 | Panel Track |
S007 | 2012-03-22 | 135 Review Track For 30-day Notice |
S006 | 2011-06-14 | 30-day Notice |
S005 | 2011-04-27 | Normal 180 Day Track No User Fee |
S004 | 2011-04-27 | 30-day Notice |
S003 | 2011-04-26 | 30-day Notice |
S002 | 2011-04-21 | 30-day Notice |
S001 | 2011-04-05 | 30-day Notice |