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.
Approval for the intrastent doublestrut stent. The device is indicated for improving luminal diameter in patients with symptomatic atherosclerotic disease of the common and/or external iliac arteries up to 100 mm in length, with a 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 | 2003-09-30 |
Decision Date | 2004-06-08 |
Notice Date | 2004-06-14 |
PMA | P030045 |
Supplement | S |
Product Code | NIO |
Docket Number | 04M-0259 |
Advisory Committee | Cardiovascular |
Expedited Review | No |
Combination Product | No |
Applicant Address | MEDTRONIC VASCULAR INC 3033 Campus Drive plymouth, MN 55441 |
Summary: | Summary of Safety and Effectiveness |
Labeling: | Labeling |
Approval Order: | Approval Order |
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 |