ABSOLUTE PRO VASCULAR STENT SYSTEMS

Stent, Iliac

FDA Premarket Approval P110028 S014

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

Implement an alternate digestion system used to prepare purchased stainless steel samples for chemical characterization.

DeviceABSOLUTE PRO VASCULAR STENT SYSTEMS
Classification NameStent, Iliac
Generic NameStent, Iliac
ApplicantABBOTT VASCULAR INC.
Date Received2015-01-14
Decision Date2015-02-06
PMAP110028
SupplementS014
Product CodeNIO
Advisory CommitteeCardiovascular
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product Yes
Applicant Address ABBOTT VASCULAR INC. 3200 Lakeside Drive santa Clara, CA 92054

Supplemental Filings

Supplement NumberDateSupplement Type
P110028Original Filing
S023 2022-11-21 135 Review Track For 30-day Notice
S022 2021-09-20 30-day Notice
S021 2020-08-05 30-day Notice
S020 2019-07-05 30-day Notice
S019 2018-06-26 30-day Notice
S018 2017-03-21 30-day Notice
S017 2017-03-16 30-day Notice
S016 2015-04-07 135 Review Track For 30-day Notice
S015 2015-02-24 30-day Notice
S014 2015-01-14 30-day Notice
S013 2014-07-18 30-day Notice
S012 2014-05-07 135 Review Track For 30-day Notice
S011 2013-08-16 135 Review Track For 30-day Notice
S010 2013-08-14 30-day Notice
S009 2013-07-29 30-day Notice
S008 2013-05-31 30-day Notice
S007 2013-01-14 30-day Notice
S006 2012-12-19 30-day Notice
S005 2012-10-15 30-day Notice
S004 2012-06-13 30-day Notice
S003 2012-05-24 30-day Notice
S002 2012-05-21 30-day Notice
S001 2012-05-11 30-day Notice

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