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 a design modification to the intrastent doublestrut stent system. The device, as modified, will be marketed under the trade name visi-pro balloon-expandable peripheral stent system and is indicated for improving luminal diameter in patients with atherosclerotic disease of the common and/or external iliac arteries up to 100 mm in length, witha reference vessel diameter of 5 to 10 mm.
Device | INTRASTENT DOUBLESTRUT STENT |
Classification Name | Stent, Iliac |
Generic Name | Stent, Iliac |
Applicant | MEDTRONIC VASCULAR INC |
Date Received | 2013-10-30 |
Decision Date | 2015-04-16 |
PMA | P030045 |
Supplement | S002 |
Product Code | NIO |
Advisory Committee | Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/components/specifications/material |
Expedited Review | No |
Combination Product | No |
Applicant Address | MEDTRONIC VASCULAR INC 3033 Campus Drive plymouth, MN 55441 |
Supplement Number | Date | Supplement Type |
---|---|---|
P030045 | Original Filing | |
S006 | 2021-04-08 | 30-day Notice |
S005 | 2019-05-03 | 30-day Notice |
S004 | 2017-11-03 | 30-day Notice |
S003 | ||
S002 | 2013-10-30 | Normal 180 Day Track |
S001 | 2005-07-18 | Normal 180 Day Track No User Fee |