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 manufacturing site located at ev3, inc. , plymouth, minnesota and a new sterilization site located at steris isomedix services, inc. Minneapolis, minnesota.
| Device | INTRASTENT DOUBLE STRUT STENT |
| Classification Name | Stent, Iliac |
| Generic Name | Stent, Iliac |
| Applicant | MEDTRONIC VASCULAR INC |
| Date Received | 2005-07-18 |
| Decision Date | 2006-02-28 |
| PMA | P030045 |
| Supplement | S001 |
| Product Code | NIO |
| 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 |
| 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 |