Wallstent (Venous) Endoprosthesis With Unistep Plus Delivery System

FDA Premarket Approval P980033 S057

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

Use of an alternate extrusion line

DeviceWallstent (Venous) Endoprosthesis With Unistep Plus Delivery System
Generic NameStent, Central Venous
ApplicantBOSTON SCIENTIFIC CORPORATION
Date Received2020-06-16
Decision Date2020-06-25
PMAP980033
SupplementS057
Product CodeQKJ 
Advisory CommitteeCardiovascular
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address BOSTON SCIENTIFIC CORPORATION one Scimed Place maple Grove, MN 55311-1566

Supplemental Filings

Supplement NumberDateSupplement Type
P980033Original Filing
S057 2020-06-16 30-day Notice
S056 2019-09-30 30-day Notice
S055 2019-06-27 30-day Notice
S054 2019-05-03 30-day Notice
S053 2019-03-22 30-day Notice
S052 2018-11-21 30-day Notice
S051 2018-11-21 30-day Notice
S050
S049 2017-06-19 30-day Notice
S048 2017-06-01 30-day Notice
S047 2016-10-03 30-day Notice
S046 2016-09-13 30-day Notice
S045 2016-07-26 30-day Notice
S044
S043 2015-03-09 Real-time Process
S042
S041 2014-04-25 30-day Notice
S040 2013-11-26 30-day Notice
S039 2013-11-25 30-day Notice
S038 2013-11-04 30-day Notice
S037 2013-09-20 30-day Notice
S036 2013-08-29 30-day Notice
S035 2013-06-19 30-day Notice
S034 2013-06-10 30-day Notice
S033 2013-05-28 30-day Notice
S032 2013-05-09 30-day Notice
S031 2013-03-21 30-day Notice
S030 2013-01-15 30-day Notice
S029 2012-11-27 135 Review Track For 30-day Notice
S028 2012-11-19 30-day Notice
S027 2012-11-19 30-day Notice
S026 2012-10-15 30-day Notice
S025 2012-09-28 30-day Notice
S024 2012-09-05 30-day Notice
S023 2012-08-13 30-day Notice
S022 2012-06-15 30-day Notice
S021 2012-06-13 30-day Notice
S020 2012-04-18 30-day Notice
S019 2011-07-07 30-day Notice
S018 2011-02-10 135 Review Track For 30-day Notice
S017 2010-04-08 135 Review Track For 30-day Notice
S016 2010-01-26 30-day Notice
S015 2008-11-19 30-day Notice
S014 2006-05-09 30-day Notice
S013 2005-03-14 Normal 180 Day Track No User Fee
S012 2004-12-20 30-day Notice
S011 2004-06-25 30-day Notice
S010 2004-04-09 30-day Notice
S009 2003-12-08 30-day Notice
S008 2003-11-17 Normal 180 Day Track No User Fee
S007 2003-08-14 30-day Notice
S006 2003-03-12 Special (immediate Track)
S005 2002-12-18 30-day Notice
S004 2002-12-12 30-day Notice
S003 2002-05-29 30-day Notice
S002 2002-04-24 Normal 180 Day Track
S001 2001-12-20 Normal 180 Day Track

NIH GUDID Devices

Device IDPMASupp
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08714729979500 P980033 050
08714729979494 P980033 050
08714729979487 P980033 050
08714729979470 P980033 050
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08714729979517 P980033 050
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08714729979531 P980033 050
08714729979630 P980033 050
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08714729979579 P980033 050
08714729979562 P980033 050
08714729979555 P980033 050
08714729979548 P980033 050
08714729979401 P980033 050

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