VENASEAL CLOSURE SYSTEM

Agent, Occluding, Vascular, Permanent

FDA Premarket Approval P140018 S004

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 an alternate site located at medtronic, ireland, parkmore business park, west galway, ireland, to perform finished device final release activities.

DeviceVENASEAL CLOSURE SYSTEM
Classification NameAgent, Occluding, Vascular, Permanent
Generic NameAgent, Occluding, Vascular, Permanent
ApplicantMEDTRONIC VASCULAR INC
Date Received2016-09-07
Decision Date2016-10-21
PMAP140018
SupplementS004
Product CodePJQ
Advisory CommitteeCardiovascular
Supplement TypeNormal 180 Day Track No User Fee
Supplement ReasonLocation Change - Manufacturer/sterilizer/packager/supplier
Expedited ReviewNo
Combination Product No
Applicant Address MEDTRONIC VASCULAR INC 3033 Campus Drive plymouth, MN 55441

Supplemental Filings

Supplement NumberDateSupplement Type
P140018Original Filing
S036 2022-11-29 30-day Notice
S035 2022-10-12 30-day Notice
S034 2022-08-15 30-day Notice
S033
S032 2022-04-29 Real-time Process
S031 2022-01-21 30-day Notice
S030 2021-11-30 30-day Notice
S029
S028 2021-09-23 30-day Notice
S027
S026
S025 2021-04-23 Special (immediate Track)
S024
S023 2021-02-25 30-day Notice
S022
S021 2020-10-19 Real-time Process
S020 2020-08-24 30-day Notice
S019 2020-03-10 Special (immediate Track)
S018 2019-10-28 Normal 180 Day Track
S017 2019-09-25 Real-time Process
S016 2019-08-09 30-day Notice
S015 2019-05-24 30-day Notice
S014 2018-11-16 30-day Notice
S013 2018-09-24 30-day Notice
S012 2018-08-10 30-day Notice
S011 2018-03-27 30-day Notice
S010 2018-03-05 30-day Notice
S009 2018-02-26 30-day Notice
S008 2017-08-04 Normal 180 Day Track
S007 2017-06-13 Special (immediate Track)
S006 2017-05-18 Normal 180 Day Track No User Fee
S005 2016-11-01 30-day Notice
S004 2016-09-07 Normal 180 Day Track No User Fee
S003 2016-07-26 30-day Notice
S002 2016-06-27 30-day Notice
S001 2015-07-28 Real-time Process

NIH GUDID Devices

Device IDPMASupp
10884521539921 P140018 000
20643169986262 P140018 006
00763000240776 P140018 018

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