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Searching News Database:  superficial femoral artery 

 HSMN NewsFeed - 2 Oct 2023
MedAlliance Acquired by Cordis for up to USD 1.135 Billion
Devices Interventional Cardiology Mergers & Acquisitions
 HSMN NewsFeed - 14 Sep 2023
MedAlliance Announces Enrollment of over 1,660 Patients in Landmark SELUTION DeNovo Study
Devices Interventional Cardiology
 HSMN NewsFeed - 31 May 2023
Excellent 12-Month Results from SELUTION SFA Trial Presented at JET
Devices Interventional
 HSMN NewsFeed - 14 Mar 2023
Over 1,000 Patients Enrolled in Landmark SELUTION DeNovo Study
Devices Interventional Cardiology
 HSMN NewsFeed - 25 Jan 2023
MedAlliance leads US Sirolimus DEB race: First US Patient enrolled into SELUTION SLR Coronary Sirolimus DEB Study
Devices Interventional Cardiology
 HSMN NewsFeed - 11 Jan 2023
MedAlliance SELUTION SLR is the first DEB to receive coronary de novo IDE approval, its fourth FDA IDE DEB Approval
Devices Interventional Cardiology FDA
 HSMN NewsFeed - 25 Oct 2022
MedAlliance SELUTION SLR Receives Coronary FDA IDE Approval
Devices Interventional Cardiology FDA
 HSMN NewsFeed - 18 Oct 2022
Cordis Announces Acquisition of MedAlliance, Positioning Itself for Market Leadership in Drug-Eluting Balloon Technology
Devices Drug Delivery Mergers & Acquisitions
 HSMN NewsFeed - 2 Nov 2020
Boston Scientific Receives FDA Approval for the Ranger(TM) Drug-Coated Balloon
Devices Interventional FDA Product Launch
 HSMN NewsFeed - 2 May 2019
Concept Medical Inc. Granted 'Breakthrough Device Designation' From FDA for Its MagicTouch Sirolimus Coated Balloon
Devices Interventional Cardiology FDA
 HSMN NewsFeed - 24 Sep 2018
Boston Scientific Receives U.S. FDA Approval for the Eluvia(TM) Drug-Eluting Vascular Stent System
Devices Interventional FDA
 HSMN NewsFeed - 15 Jun 2018
Medtronic Receives FDA Approval for 200mm & 250mm IN.PACT(TM) Admiral(TM) Drug Coated Balloons
Devices Interventional FDA
 HSMN NewsFeed - 27 Feb 2018
Abbott and Surmodics Announce Agreement for Next-Generation Drug-Coated Balloon
Devices Interventional Licensing
 HSMN NewsFeed - 22 Aug 2017
Getinge announces full U.S. availability of Pulsar(R)-18 self-expanding stent from BIOTRONIK for patients with peripheral artery disease
Devices Interventional Product Launch
 HSMN NewsFeed - 3 Jul 2017
BIOTRONIK US Announces Pivotal Trial Results of the Pulsar-18 Stent with 4-French Delivery System
Devices Interventional
 HSMN NewsFeed - 20 Oct 2016
Akesys Medical and Elixir Medical Announce First Human Implant of the PRAVA(TM) Bioresorbable Scaffold for Peripheral Vascular Disease
Devices Interventional
 HSMN NewsFeed - 2 Aug 2016
GORE(R) TIGRIS(R) Vascular Stent Gains FDA Approval for Treatment of Peripheral Artery Disease
Devices Interventional FDA
 HSMN NewsFeed - 28 Jun 2016
GORE(R) VIABAHN(R) Endoprosthesis Found to Provide Superior Patency and Reduced Interventions Versus Balloon Angioplasty Alone for Challenging AV Access Cases
Devices Interventional
 HSMN NewsFeed - 22 Feb 2016
Boston Scientific Receives CE Mark For Eluvia(TM) Drug-Eluting Vascular Stent and Announces Initiation of New Clinical Trial
Devices Interventional Regulatory Product Launch
 HSMN NewsFeed - 19 May 2015
Shockwave Medical Announces $40 Million in Funding for Novel Lithoplasty System to Treat Advanced Peripheral, Coronary Vascular and Aortic Valve Disease
Devices Interventional Cardiology Venture Capital
 HSMN NewsFeed - 29 Apr 2015
Intact Vascular’s First-In-Man Clinical Study Results Published in the Journal of the American College Of Cardiology: Cardiovascular Interventions
Devices Interventional
 HSMN NewsFeed - 10 Dec 2014
Gore Receives CE Mark Approval for GORE(R) VIABAHN(R) Endoprosthesis for Revision of Arteriovenous Access
Devices Regulatory
 HSMN NewsFeed - 15 Aug 2014
Cook Medical Enrolls First Patient in Zilver(R) PTX(R) Drug Eluting Peripheral Stent Clinical Study in China
Devices Interventional
 HSMN NewsFeed - 5 Jun 2014
Cook Medical Makes Zilver(R) PTX(R) Drug-Eluting Stent Available in Canada
Devices Interventional
 HSMN NewsFeed - 17 Mar 2014
BioCardia(R) Receives CE Mark for Morph AccessPro(TM) Steerable Introducer
Devices Interventional Cardiology Regulatory
 HSMN NewsFeed - 20 Feb 2014
Gore REVISE Clinical Study Demonstrates Superiority of GORE VIABAHN Endoprosthesis
Devices
 HSMN NewsFeed - 29 Jan 2014
Bioheart Announces First Adipose Derived Stem Cell Implantation in Azerbaijan
Regnerative Medicine
 HSMN NewsFeed - 6 Nov 2013
Gore Receives FDA Approval for 25 cm GORE(R) VIABAHN(R) Endoprosthesis
Devices Interventional FDA
 HSMN NewsFeed - 24 Sep 2013
FDA Approves Medtronic's Complete 'SE' Vascular Stent for Use in Superficial Femoral and Proximal Popliteal (Leg) Arteries
Devices Interventional FDA
 HSMN NewsFeed - 21 Aug 2013
Abbott Completes Acquisition of IDEV Technologies
Devices Interventional Mergers & Acquisitions
 HSMN NewsFeed - 15 Jul 2013
Abbott to Acquire IDEV Technologies to Expand Global Peripheral Technology Portfolio
Devices Interventional Mergers & Acquisitions
 HSMN NewsFeed - 12 Mar 2013
Cordis Acquires Flexible Stenting Solutions, Inc.
Devices Interventional Mergers & Acquisitions
 HSMN NewsFeed - 31 Jan 2013
IDEV Announces Results from Revascularization with Supera on Real World Patients (RESTORE) Study, Demonstrating Positive Clinical Outcomes in Significantly Diseased Patients with Long Lesions
Devices Interventional
 HSMN NewsFeed - 24 Jan 2013
Final Results of Spectranetics Study Supports Successful Use of Laser Atherectomy for Treating Patients With Peripheral In-Stent Restenosis
Devices Interventional
 HSMN NewsFeed - 19 Dec 2012
First U.S. Patient Treated Following FDA Approval of Cook Medical’s First-of-its-Kind Zilver(R) PTX(R) Drug-Eluting Peripheral Stent
Devices Interventional
 HSMN NewsFeed - 8 Nov 2012
S.M.A.R.T.(R) Vascular Stent Systems Receive FDA Approval for Use in SFA
Devices Interventional FDA
 HSMN NewsFeed - 11 Oct 2012
Cook Medical’s Zilver(R) PTX(R) Trial Shows Sustained Patency after Three Years
Devices Interventional
 HSMN NewsFeed - 23 May 2012
BIOTRONIK Announces Positive Results for Pulsar Stent in 4EVER Clinical Study
Devices Interventional
 HSMN NewsFeed - 21 May 2012
Cook Medical Launches First Drug-Eluting Stent in Australia to Treat Peripheral Arterial Disease (PAD)
Devices Interventional Regulatory
 HSMN NewsFeed - 16 May 2012
Medtronic IN.PACT Drug-Eluting Balloon Studies Show Significant Benefit of Novel Medical Device in Treating Narrowed Arteries
Devices Interventional Cardiology
 HSMN NewsFeed - 14 May 2012
Boston Scientific Announces CE Mark and European Launch of Innova(TM) Self-expanding Bare-metal Stent System
Devices Interventional Regulatory
 HSMN NewsFeed - 13 Apr 2012
Medtronic Initiates Landmark U.S. Drug-Eluting Balloon Study
Devices Interventional
 HSMN NewsFeed - 1 Mar 2012
Cook Medical Receives Japanese Approval to Market Its Zilver(R) PTX(R) Drug-Eluting Stent
Devices Interventional Regulatory
 HSMN NewsFeed - 2 Feb 2012
Spectranetics Announces Interim Results from German Study Treating Patients with Peripheral In-Stent Restenosis
Devices Interventional
 HSMN NewsFeed - 15 Dec 2011
Journal of Endovascular Therapy Publishes Two-Year Data On SUPERA(R) Stent Used in the Superficial Femoral Artery
Devices Interventional
 HSMN NewsFeed - 1 Dec 2011
Covidien's Embolic Protection Device Receives FDA Clearance
Devices Interventional FDA
 HSMN NewsFeed - 1 Nov 2011
Boston Scientific Announces Schedule of Events at TCT Scientific Symposium
Devices Interventional Cardiology
 HSMN NewsFeed - 18 Oct 2011
BIOTRONIK Launches First 20 mm–200 mm Stents on 4 F Platform for Treatment of SFA and BTK Disease
Devices Interventional
 HSMN NewsFeed - 8 Sep 2011
Angioslide Announces the European Launch of New 300 mm Long Device Allowing Treatment of Entire Superficial Femoral Artery(SFA) with One Device
Devices Interventional
 HSMN NewsFeed - 12 Jul 2011
IDEV Technologies Launches Lower Profile SUPERA VERITAS(R) Stent Delivery System
Devices Interventional
 HSMN NewsFeed - 13 Jun 2011
Pathway Medical Technologies Expands JETSTREAM G3 SF Family With FDA 510(k) Clearance for 1.6 mm Catheter
Devices Interventional FDA
 HSMN NewsFeed - 5 Apr 2011
Boston Scientific Begins International Clinical Trial Enrollment for INNOVA Self-Expanding Bare-Metal Stent System
Devices Interventional
 HSMN NewsFeed - 21 Mar 2011
Gore Reports First Patient Treated in the United States using GORE(R) VIABAHN(R) Endoprosthesis with Heparin Bioactive Surface on a Lower Profile Delivery System
Devices Interventional
 HSMN NewsFeed - 17 Feb 2011
Gore Announces FDA Approval of Next Evolution of GORE(R) VIABAHN(R) Endoprosthesis
Devices Interventional FDA
 HSMN NewsFeed - 26 Jan 2011
Long-Term European Data Released for SUPERA(R) Stent from IDEV Technologies
Devices Interventional
 HSMN NewsFeed - 19 Jan 2011
Gore Announces European Availability of Next Evolution of GORE(R) VIABAHN(R) Endoprosthesis
Devices Interventional
 HSMN NewsFeed - 18 Jan 2011
Covidien Unveils Next Generation EverFlex+(TM) Peripheral Stent System
Devices Interventional
 HSMN NewsFeed - 18 Jan 2011
Cook Medical’s Ongoing Drug-Eluting Peripheral Stent Trial Shows Consistent Outcomes Over 24 Months Compared to One-Year Data
Devices Interventional
 HSMN NewsFeed - 3 Nov 2010
IDEV Technologies Announces FDA 510(k) Clearance for SUPERA VERITAS
Devices Interventional FDA
 HSMN NewsFeed - 28 Sep 2010
Medtronic Advances Research on Drug-Eluting Balloons for Coronary and Peripheral Artery Disease
Devices Interventional Cardiology
 HSMN NewsFeed - 23 Sep 2010
First European Patients Treated for Peripheral Artery Disease Using Longest Length GORE(R) VIABAHN(R) Endoprosthesis
Devices Interventional
 HSMN NewsFeed - 9 Sep 2010
Terumo Medical Corporation Announces First U.S. Patient Implant in Landmark Pilot Study Simultaneously Enrolling in the U.S. & Japan
Devices Interventional
 HSMN NewsFeed - 6 Aug 2010
Medtronic Completes Enrollment in Clinical Study of Complete SE(R) (Self-Expanding) Vascular Stent
Devices Interventional
 HSMN NewsFeed - 1 Jul 2010
Gore Receives CE Mark for Longer Length GORE(R) VIABAHN(R) Endoprosthesis
Devices Interventional Regulatory
 HSMN NewsFeed - 11 Jun 2010
Cook Medical Files Pre-Market Approval Application for FDA Approval of Zilver(R) PTX(R) Drug-Eluting Stent Platform
Devices Interventional
 HSMN NewsFeed - 24 May 2010
IDEV Technologies Names Veteran Healthcare Executive Dennis Donohoe, M.D. Chief Medical Officer
Devices Personnel
 HSMN NewsFeed - 18 May 2010
IDEV Technologies Announces European Launch of SUPERA VERITAS(TM) Stent Delivery System
Devices Interventional
 HSMN NewsFeed - 12 May 2010
Terumo To Simultaneously Evaluate Misago Self-Expanding Stent System in the United States and Japan
Devices Interventional FDA
 HSMN NewsFeed - 21 Apr 2010
Medtronic Receives FDA Approval for New Indication for Complete(R) SE Vascular Stent
Devices Interventional FDA
 HSMN NewsFeed - 27 Jan 2010
Invatec Completes its Maris Plus Self-Expanding Peripheral Stent System at LINC 2010
Devices Interventional
 HSMN NewsFeed - 9 Nov 2009
VIVA 2009 Late-Breaking Trials Highlight Advances in Interventional Treatments of Peripheral Arterial Disease
Devices Interventional
 HSMN NewsFeed - 21 Sep 2009
New Zilver PTX Drug-Eluting Stent from Cook Medical Could Greatly Reduce Need for Leg Amputations and Bypass Surgery for European Patients
Devices Interventional
 HSMN NewsFeed - 24 Aug 2009
IDEV(R) Technologies Announces First Patient Enrolled in Multi-Center Clinical Trial of SUPERA(R) PERipheral Stent
Devices Interventional
 HSMN NewsFeed - 11 Aug 2009
Breakthrough Drug-Eluting Stent to Treat Peripheral Arterial Disease Now Available in Europe
Devices Interventional
 HSMN NewsFeed - 11 Aug 2009
Zilver PTX Stent from Cook Medical Gains CE Mark
Devices Interventional Regulatory
 HSMN NewsFeed - 21 Jul 2009
Gore Receives FDA Approval for Next Generation of Large Diameter GORE VIABAHN(R) Endoprosthesis with Heparin Bioactive Surface
Devices Interventional FDA
 HSMN NewsFeed - 15 Jul 2009
Spectranetics Announces First Human Uses of Turbo-Tandem System
Devices Interventional
 HSMN NewsFeed - 30 Jun 2009
Gore Receives FDA Approval for Modification of GORE VIABAHN® Endoprosthesis
Devices Interventional FDA
 HSMN NewsFeed - 19 May 2009
Invatec Receives CE Mark Approval for the IN.PACT Admiral Drug Eluting Balloon
Devices Interventional Regulatory
 HSMN NewsFeed - 5 Jan 2009
Medtronic Announces Clinical Trial of Stent for Peripheral Arterial Disease
Devices Interventional
 HSMN NewsFeed - 17 Sep 2008
Gore Announces Broadened FDA Indication for GORE VIABAHN(R) Endoprosthesis for Iliac Occlusive Disease
Devices Interventional FDA
 HSMN NewsFeed - 15 Sep 2008
Spectranetics Provides Update on VIVA II: SALVAGE Trial
Devices Interventional
 HSMN NewsFeed - 10 Sep 2008
Cook Medical Completes Enrollment in First International Trial of First-of-Its-Kind Drug-Eluting Peripheral Stent
Devices Interventional
 HSMN NewsFeed - 2 Sep 2008
First Patient Enrolled in Study Evaluating S.M.A.R.T. (R) Nitinol Self-Expandable Stent System in Leg Disease
Devices Interventional
 HSMN NewsFeed - 1 May 2008
AngioScore Receives FDA Clearance to Market AngioSculpt PTA Scoring Balloon Catheter for Additional Peripheral Indications
Devices Interventional FDA
 HSMN NewsFeed - 25 Feb 2008
First Patient Enrolled in Study Evaluating Performance of Spectranetics Laser Ablation Followed by GORE VIABAHN(R) Endoprosthesis with Heparin Bioactive Surface
Devices Interventional
 HSMN NewsFeed - 2 Jan 2008
VIBRANT Study of GORE VIABAHN(R) Endoprosthesis Completes Enrollment
Devices Interventional
 HSMN NewsFeed - 7 Dec 2007
Edwards Lifesciences to Sell LifeStent Product Line to Bard
Devices Interventional Acquisitions
 HSMN NewsFeed - 7 Dec 2007
Bard Signs Agreement to Acquire LifeStent(R) from Edwards Lifesciences
Devices Interventional Acquisitions
 HSMN NewsFeed - 24 Oct 2007
Spectranetics Announces Clinical Data From Cello Trial
Devices Interventional
 HSMN NewsFeed - 23 Oct 2007
Edwards' Resilient Trial Demonstrates Statistically Superior Results for Treating Peripheral Arterial Disease in the Leg
Devices Interventional
 HSMN NewsFeed - 18 Oct 2007
First Patient Enrolled in Study of the GORE VIABAHN(R) Endoprosthesis with Heparin Bioactive Surface for Lower Limb Peripheral Vascular Disease
Devices Interventional
 HSMN NewsFeed - 26 Sep 2007
Spectranetics Enrolls First Patient in PATENT Trial for the Treatment of Instent Restenosis
Devices Interventional
 HSMN NewsFeed - 20 Sep 2007
LeMaitre Vascular Acquires Vascular Architects
Devices Interventional Mergers & Acquisitions
 HSMN NewsFeed - 7 Jun 2007
New Balloon Catheter Available Worldwide for Carotid and Renal Angioplasty Procedures
Devices Interventional
 HSMN NewsFeed - 4 Jun 2007
ev3 Receives Conditional IDE Approval to Study Use of Protege(R) EverFlex(TM) Self-Expanding Stent System in the Treatment of Peripheral Artery Disease
Devices Interventional FDA
 HSMN NewsFeed - 23 May 2007
Abbott Initiates First Clinical Study of Everolimus Eluting Stent System for Patients with Peripheral Arterial Disease
Devices Interventional
 HSMN NewsFeed - 18 Apr 2007
Cordis Corporation and ClearStream Technologies Group, plc, Sign Distribution Agreement for Peripheral Angioplasty Balloon Catheters
Devices Interventional Distribution
 HSMN NewsFeed - 15 Feb 2007
New Version of Devices to Treat Clogged Neck Arteries Approved by U.S. Food and Drug Administration
Devices Interventional FDA
 HSMN NewsFeed - 30 Jan 2007
First International Trial of Drug-Eluting Peripheral Artery Stent Results Encouraging
Devices Interventional
 HSMN NewsFeed - 23 Oct 2006
ev3 Inc. Issues Durability Guarantee for its EverFlex(TM) Self-Expanding Stents
Devices Interventional
 HSMN NewsFeed - 26 Sep 2006
U.S. Food and Drug Administration Approves New Medical Devices to Treat Clogged Neck Arteries
Devices Interventional FDA
 HSMN NewsFeed - 6 Sep 2006
First Drug-Eluting Stent Approved in Europe for Most Severe Form of Arterial Disease in the Leg
Devices Interventional Regulatory
 HSMN NewsFeed - 20 Jul 2006
Spectranetics Announces First Patient Enrolled in CELLO Trial
Devices Interventional
 HSMN NewsFeed - 27 Jun 2006
Peripheral Rinspiration(R) Catheter System Prominently Featured at Mount Sinai Live Cardiovascular Symposium
Devices Interventional
 HSMN NewsFeed - 1 Jun 2006
Kerberos Completes First Clinical Cases with New Peripheral Rinspiration(R) System
Devices
 HSMN NewsFeed - 31 May 2006
Cordis Announces Nationwide Introduction of Breakthrough Devices to Treat Artery Blockages in Leg
Devices Interventional
 HSMN NewsFeed - 19 May 2006
Spectranetics CLiRpath(R) TURBO-Booster(TM) Featured in Live Case at EuroPCR
Devices Interventional
 HSMN NewsFeed - 16 May 2006
Physicians Now Have a New Treatment Option for Patients With a Common Vascular Disease Affecting the Legs
Devices Interventional
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