INTRASTENT DOUBLESTRUT STENT

Stent, Iliac

FDA Premarket Approval P030045 S002

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.

Pre-market Approval Supplement Details

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.

DeviceINTRASTENT DOUBLESTRUT STENT
Classification NameStent, Iliac
Generic NameStent, Iliac
ApplicantMEDTRONIC VASCULAR INC
Date Received2013-10-30
Decision Date2015-04-16
PMAP030045
SupplementS002
Product CodeNIO
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address MEDTRONIC VASCULAR INC 3033 Campus Drive plymouth, MN 55441

Supplemental Filings

Supplement NumberDateSupplement Type
P030045Original 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

NIH GUDID Devices

Device IDPMASupp
00643169787568 P030045 002
00643169787704 P030045 002
00643169787711 P030045 002
00643169787728 P030045 002
00643169787735 P030045 002
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00643169787759 P030045 002
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00643169787629 P030045 002
00643169787636 P030045 002
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00643169788022 P030045 002
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00643169787896 P030045 002
00643169787902 P030045 002
00643169787919 P030045 002
00643169787926 P030045 002
00643169788060 P030045 002

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