Abbott Vascular Idef Technologies Inc

FDA Filings

This page includes the latest FDA filings for Abbott Vascular Idef Technologies Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P120020S027 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2021-09-30
PMA P120020S026 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2021-05-12
PMA P120020S025 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2020-12-14
PMA P120020S024 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2020-09-30
PMA P120020S023 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2019-06-13
PMA P120020S022 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2019-03-14
PMA P120020S021 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2019-02-20
PMA P120020S020 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System, Supera Pro Interwoven Peripheral Stent System	2018-10-04
PMA P120020S019 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Self-Expanding Stent System	2018-09-20
PMA P120020S018 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Pro Interwoven Peripheral Stent System	2018-07-26
PMA P120020S017 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2018-01-25
PMA P120020S016 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	Supera Peripheral Stent System	2017-07-14
PMA P120020S014 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2017-02-01
PMA P120020S015 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2016-10-06
PMA P120020S013 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2016-07-13
PMA P120020S011 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2016-01-22
PMA P120020S012 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2015-12-16
PMA P120020S009 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2015-07-24
PMA P120020S010 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2015-06-10
PMA P120020S008 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2015-05-12
PMA P120020S007 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2015-03-06
PMA P120020S006 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2015-01-09
PMA P120020S003 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2014-11-07
PMA P120020S002 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM (SUPERB)	2014-10-20
PMA P120020S005 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2014-09-02
PMA P120020S004 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2014-07-10
PMA P120020S001 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2014-04-30
PMA P120020 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)	SUPERA PERIPHERAL STENT SYSTEM	2014-03-28

Similar & Related FDA Registered Companies

• ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP120020 Supplement NumberS030 Date Received11/21/2022 Decision Date01/31/2023 Product Code NIP  Advisory Committee Cardiovascular Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP120020 Supplement NumberS029 Date Received09/30/2022 Decision Date12/20/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Typereal-time Process Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP120020 Supplement NumberS028 Date Received09/30/2022 Decision Date11/22/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Typereal-time Process Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No