EverFlex Self-Expanding Peripheral Stent System, EverFlex Self-Expanding Peripheral Stent System with Entrust Delivery S

FDA Premarket Approval P110023 S035

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

DeviceEverFlex Self-Expanding Peripheral Stent System, EverFlex Self-Expanding Peripheral Stent System with Entrust Delivery S
Generic NameStent, Superficial Femoral Artery
ApplicantMEDTRONIC VASCULAR INC3033 Campus Driveplymouth, MN 55441 PMA NumberP110023 Supplement NumberS035 Date Received05/25/2022 Decision Date06/03/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Date Received2022-05-25
Decision Date2022-06-03
PMAP110023
SupplementS035
Product CodeNIP 
Advisory CommitteeCardiovascular
Supplement Type30-day Notice
Supplement ReasonProcess Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination ProductNo
Applicant AddressMEDTRONIC VASCULAR INC
3033 Campus Drive
plymouth, MN 55441 PMA NumberP110023 Supplement NumberS035 Date Received05/25/2022 Decision Date06/03/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No Combination ProductNo Approval Order Statement  
the Addition Of A Rolling Mill Machine At A Supplier Site

Supplemental Filings

Supplement NumberDateSupplement Type
P110023Original Filing
S036 2022-11-15 30-day Notice
S035 2022-05-25 30-day Notice
S034
S033 2021-12-13 30-day Notice
S032 2021-04-08 30-day Notice
S031 2020-12-10 30-day Notice
S030 2020-07-21 30-day Notice
S029 2020-05-06 Real-time Process
S028 2019-08-27 Normal 180 Day Track No User Fee
S027 2019-05-24 30-day Notice
S026 2019-05-03 30-day Notice
S025 2019-02-19 30-day Notice
S024 2017-11-03 30-day Notice
S023 2016-12-07 30-day Notice
S022 2016-11-02 30-day Notice
S021 2016-09-28 Normal 180 Day Track No User Fee
S020 2016-07-05 30-day Notice
S019 2016-06-06 30-day Notice
S018 2016-03-22 30-day Notice
S017
S016 2015-11-20 30-day Notice
S015 2015-03-23 135 Review Track For 30-day Notice
S014 2015-03-15 30-day Notice
S013 2014-11-17 30-day Notice
S012 2014-08-22 Normal 180 Day Track
S011 2014-07-21 30-day Notice
S010 2014-07-10 Normal 180 Day Track No User Fee
S009 2014-06-05 30-day Notice
S008 2014-06-03 30-day Notice
S007 2014-04-14 Panel Track
S006 2014-02-03 Normal 180 Day Track No User Fee
S005
S004 2012-10-09 30-day Notice
S003 2012-06-11 30-day Notice
S002 2012-05-16 30-day Notice
S001 2012-04-24 30-day Notice

NIH GUDID Devices

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