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HSMN NewsFeed - 15 Sep 2022
Excision Medical Inc. Announces $2.5M Funding and Two Important Additions to its Scientific Advisory Board
Excision Medical Inc. Announces $2.5M Funding and Two Important Additions to its Scientific Advisory Board
HSMN NewsFeed - 7 Mar 2018
Contego Medical Announces the Start of Enrollment in the PERFORMANCE I Trial
Contego Medical Announces the Start of Enrollment in the PERFORMANCE I Trial
HSMN NewsFeed - 18 Jul 2016
Essential Medical Inc. Announces CE Mark Approval for the MANTA(TM) Large Bore Vascular Closure Device
Essential Medical Inc. Announces CE Mark Approval for the MANTA(TM) Large Bore Vascular Closure Device
HSMN NewsFeed - 20 Oct 2015
Silk Road Medical Announces up to $57 Million in New Funding for Novel Approach to Preventing Strokes
Silk Road Medical Announces up to $57 Million in New Funding for Novel Approach to Preventing Strokes
HSMN NewsFeed - 19 May 2015
FDA Grants Premarket Approval for Silk Road Medical's ENROUTE(R) Transcarotid Stent System
FDA Grants Premarket Approval for Silk Road Medical's ENROUTE(R) Transcarotid Stent System
HSMN NewsFeed - 10 Feb 2015
Silk Road Medical Announces FDA 510(k) Clearance of the ENROUTE(R) Transcarotid Neuroprotection System
Silk Road Medical Announces FDA 510(k) Clearance of the ENROUTE(R) Transcarotid Neuroprotection System
HSMN NewsFeed - 12 Sep 2013
First Patient Enrolled in Gore SCAFFOLD Clinical Study for Carotid Stenting
First Patient Enrolled in Gore SCAFFOLD Clinical Study for Carotid Stenting
HSMN NewsFeed - 12 Jul 2011
Boston Scientific Completes Clinical Trial Enrollment for Adapt Monorail Carotid Stent System
Boston Scientific Completes Clinical Trial Enrollment for Adapt Monorail Carotid Stent System
HSMN NewsFeed - 15 Jun 2011
Cordis Announces Discontinuation of NEVO Sirolimus-Eluting Coronary Stent
Cordis Announces Discontinuation of NEVO Sirolimus-Eluting Coronary Stent
HSMN NewsFeed - 23 Oct 2009
Invatec Receives FDA Clearance for Mo.Ma(R) Ultra Proximal Cerebral Protection Device
Invatec Receives FDA Clearance for Mo.Ma(R) Ultra Proximal Cerebral Protection Device
HSMN NewsFeed - 1 Apr 2009
Abbott Initiates U.S. Study of Absolute Pro(TM) Peripheral Stent System for Iliac Artery Disease
Abbott Initiates U.S. Study of Absolute Pro(TM) Peripheral Stent System for Iliac Artery Disease
HSMN NewsFeed - 10 Mar 2009
Gore Announces First Patient Treated With Recently-Cleared GORE Flow Reversal System
Gore Announces First Patient Treated With Recently-Cleared GORE Flow Reversal System
HSMN NewsFeed - 10 Oct 2008
W. L. Gore & Associates Receives FDA Approval for Gore EMBOLDEN Clinical Study
W. L. Gore & Associates Receives FDA Approval for Gore EMBOLDEN Clinical Study
HSMN NewsFeed - 5 May 2008
Gore Receives Approval From FDA For Unique Patent Foramen Ovale Stroke Study
Gore Receives Approval From FDA For Unique Patent Foramen Ovale Stroke Study
HSMN NewsFeed - 23 Oct 2007
Boston Scientific Carotid Artery Stenting Trials Produce Positive Three-Year Results
Boston Scientific Carotid Artery Stenting Trials Produce Positive Three-Year Results
HSMN NewsFeed - 23 Oct 2007
Next Generation Devices to Treat Clogged Neck Arteries Launched in U.S. and Europe
Next Generation Devices to Treat Clogged Neck Arteries Launched in U.S. and Europe
HSMN NewsFeed - 15 Feb 2007
New Version of Devices to Treat Clogged Neck Arteries Approved by U.S. Food and Drug Administration
New Version of Devices to Treat Clogged Neck Arteries Approved by U.S. Food and Drug Administration
HSMN NewsFeed - 6 Feb 2007
Abbott Statement Regarding CMS' Proposed Expansion of Coverage for Carotid Artery Stenting
Abbott Statement Regarding CMS' Proposed Expansion of Coverage for Carotid Artery Stenting
HSMN NewsFeed - 14 Dec 2006
FilterWire EZ(TM) Embolic Protection System Cleared By FDA For Carotid Artery Stenting
FilterWire EZ(TM) Embolic Protection System Cleared By FDA For Carotid Artery Stenting
HSMN NewsFeed - 14 Nov 2006
Kensey Nash Announces Commencement of Carotid Pivotal Trial for TriActiv ProGuard System
Kensey Nash Announces Commencement of Carotid Pivotal Trial for TriActiv ProGuard System
HSMN NewsFeed - 3 Nov 2006
Boston Scientific Announces FDA Approval of NexStent(R) Carotid Artery Stenting System
Boston Scientific Announces FDA Approval of NexStent(R) Carotid Artery Stenting System
HSMN NewsFeed - 23 Oct 2006
Boston Scientific Reports Positive Results for its Carotid Artery Stenting Trial
Boston Scientific Reports Positive Results for its Carotid Artery Stenting Trial
HSMN NewsFeed - 27 Sep 2006
Medtronic Achieves Key Milestones in Rapidly Growing Peripheral Vascular Business
Medtronic Achieves Key Milestones in Rapidly Growing Peripheral Vascular Business
HSMN NewsFeed - 26 Sep 2006
U.S. Food and Drug Administration Approves New Medical Devices to Treat Clogged Neck Arteries
U.S. Food and Drug Administration Approves New Medical Devices to Treat Clogged Neck Arteries
HSMN NewsFeed - 13 Sep 2006
Abbott Announces European Launch of Next-Generation Device Designed to Treat Patients at Risk of Stroke
Abbott Announces European Launch of Next-Generation Device Designed to Treat Patients at Risk of Stroke
HSMN NewsFeed - 12 Jul 2006
Kensey Nash Receives FDA 510(k) Clearance for TriActiv FX(R) Embolic Protection System
Kensey Nash Receives FDA 510(k) Clearance for TriActiv FX(R) Embolic Protection System
HSMN NewsFeed - 26 Apr 2006
Kensey Nash Announces Completion of Carotid Pilot Trial Using the TriActiv(R) ProGuard(TM) System
Kensey Nash Announces Completion of Carotid Pilot Trial Using the TriActiv(R) ProGuard(TM) System
HSMN NewsFeed - 7 Mar 2006
Kensey Nash Announces Low 3.2% MACE Rate Achieved Using New TriActiv FX(R) Embolic Protection System
Kensey Nash Announces Low 3.2% MACE Rate Achieved Using New TriActiv FX(R) Embolic Protection System
HSMN NewsFeed - 17 Feb 2006
ev3 Receives FDA Clearance for SpideRX(TM) Embolic Protection Device for Carotid Artery Stenting
ev3 Receives FDA Clearance for SpideRX(TM) Embolic Protection Device for Carotid Artery Stenting
HSMN NewsFeed - 15 Feb 2006
Kensey Nash Receives CE Mark Approval for New TriActiv(R) ProGuard(TM) Embolic Protection System
Kensey Nash Receives CE Mark Approval for New TriActiv(R) ProGuard(TM) Embolic Protection System
HSMN NewsFeed - 23 Jan 2006
Kensey Nash Submits TriActiv FX(R) Embolic Protection System 510(k) Application to FDA
Kensey Nash Submits TriActiv FX(R) Embolic Protection System 510(k) Application to FDA
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