Approval for an alternate site located at medtronic, ireland, parkmore business park, west galway, ireland, to perform finished device final release activities.
Device | VENASEAL CLOSURE SYSTEM |
Classification Name | Agent, Occluding, Vascular, Permanent |
Generic Name | Agent, Occluding, Vascular, Permanent |
Applicant | MEDTRONIC VASCULAR INC |
Date Received | 2016-09-07 |
Decision Date | 2016-10-21 |
PMA | P140018 |
Supplement | S004 |
Product Code | PJQ |
Advisory Committee | Cardiovascular |
Supplement Type | Normal 180 Day Track No User Fee |
Supplement Reason | Location Change - Manufacturer/sterilizer/packager/supplier |
Expedited Review | No |
Combination Product | No |
Applicant Address | MEDTRONIC VASCULAR INC 3033 Campus Drive plymouth, MN 55441 |
Supplemental Filings
Supplement Number | Date | Supplement Type |
P140018 | | Original Filing |
S036 |
2022-11-29 |
30-day Notice |
S035 |
2022-10-12 |
30-day Notice |
S034 |
2022-08-15 |
30-day Notice |
S033 | | |
S032 |
2022-04-29 |
Real-time Process |
S031 |
2022-01-21 |
30-day Notice |
S030 |
2021-11-30 |
30-day Notice |
S029 | | |
S028 |
2021-09-23 |
30-day Notice |
S027 | | |
S026 | | |
S025 |
2021-04-23 |
Special (immediate Track) |
S024 | | |
S023 |
2021-02-25 |
30-day Notice |
S022 | | |
S021 |
2020-10-19 |
Real-time Process |
S020 |
2020-08-24 |
30-day Notice |
S019 |
2020-03-10 |
Special (immediate Track) |
S018 |
2019-10-28 |
Normal 180 Day Track |
S017 |
2019-09-25 |
Real-time Process |
S016 |
2019-08-09 |
30-day Notice |
S015 |
2019-05-24 |
30-day Notice |
S014 |
2018-11-16 |
30-day Notice |
S013 |
2018-09-24 |
30-day Notice |
S012 |
2018-08-10 |
30-day Notice |
S011 |
2018-03-27 |
30-day Notice |
S010 |
2018-03-05 |
30-day Notice |
S009 |
2018-02-26 |
30-day Notice |
S008 |
2017-08-04 |
Normal 180 Day Track |
S007 |
2017-06-13 |
Special (immediate Track) |
S006 |
2017-05-18 |
Normal 180 Day Track No User Fee |
S005 |
2016-11-01 |
30-day Notice |
S004 |
2016-09-07 |
Normal 180 Day Track No User Fee |
S003 |
2016-07-26 |
30-day Notice |
S002 |
2016-06-27 |
30-day Notice |
S001 |
2015-07-28 |
Real-time Process |
NIH GUDID Devices