Wallstent Iliac Endoprostehsis with Unistep Plus Delivery System

Stent, Iliac

FDA Premarket Approval P940019 S055

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

To add an alternate external process challenge device (epcd) to the 40°c sterilization cycle

DeviceWallstent Iliac Endoprostehsis with Unistep Plus Delivery System
Classification NameStent, Iliac
Generic NameStent, Iliac
ApplicantBOSTON SCIENTIFIC SCIMED, INC.
Date Received2019-05-03
Decision Date2019-05-30
PMAP940019
SupplementS055
Product CodeNIO
Advisory CommitteeCardiovascular
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address BOSTON SCIENTIFIC SCIMED, INC. one Scimed Place maple Grove, MN 55311-1566

Supplemental Filings

Supplement NumberDateSupplement Type
P940019Original Filing
S062 2022-11-14 30-day Notice
S061 2022-10-27 30-day Notice
S060 2022-06-03 30-day Notice
S059 2020-07-10 30-day Notice
S058 2020-06-16 30-day Notice
S057 2019-09-30 30-day Notice
S056 2019-06-27 30-day Notice
S055 2019-05-03 30-day Notice
S054 2019-03-22 30-day Notice
S053 2018-11-21 30-day Notice
S052 2018-11-21 30-day Notice
S051 2017-06-19 30-day Notice
S050 2017-06-01 30-day Notice
S049 2016-10-03 30-day Notice
S048 2016-09-13 30-day Notice
S047 2016-07-26 30-day Notice
S046
S045
S044 2014-04-25 30-day Notice
S043 2013-11-26 30-day Notice
S042 2013-11-25 30-day Notice
S041 2013-09-20 30-day Notice
S040 2013-08-29 30-day Notice
S039 2013-06-10 30-day Notice
S038 2013-05-28 30-day Notice
S037 2013-05-09 30-day Notice
S036 2013-03-21 30-day Notice
S035 2012-11-27 135 Review Track For 30-day Notice
S034 2012-11-19 30-day Notice
S033 2012-11-19 30-day Notice
S032 2012-10-15 30-day Notice
S031 2012-09-28 30-day Notice
S030 2012-09-05 30-day Notice
S029 2012-08-13 30-day Notice
S028 2012-06-15 30-day Notice
S027 2012-06-13 30-day Notice
S026 2011-07-07 30-day Notice
S025 2011-06-20 Real-time Process
S024 2011-02-10 135 Review Track For 30-day Notice
S023 2010-04-08 135 Review Track For 30-day Notice
S022 2010-01-26 30-day Notice
S021 2007-08-13 Special (immediate Track)
S020 2006-05-09 30-day Notice
S019 2005-03-14 Normal 180 Day Track No User Fee
S018 2004-12-20 30-day Notice
S017 2003-12-08 30-day Notice
S016 2003-11-17 Normal 180 Day Track No User Fee
S015 2003-08-14 30-day Notice
S014 2002-12-18 30-day Notice
S013 2002-12-12 30-day Notice
S012 2002-05-29 30-day Notice
S011 2002-04-24 Normal 180 Day Track
S010 2002-01-09 Special (immediate Track)
S009 2001-12-20 Normal 180 Day Track
S008 2001-07-12 Special (immediate Track)
S007 2001-05-03 30-day Notice
S006
S005 1999-09-01 Normal 180 Day Track
S004 1998-09-14 Normal 180 Day Track
S003 1996-12-23 Normal 180 Day Track
S002 1996-10-15 Normal 180 Day Track
S001

NIH GUDID Devices

Device IDPMASupp
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