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Searching News Database:  Femoropopliteal 

 HSMN NewsFeed - 31 Mar 2026
SirPAD: Primary Results Confirm the Safety and Efficacy of Sirolimus Coated Balloon in PAD
Devices Interventional Cardiology
 HSMN NewsFeed - 7 Jan 2025
Concept Medical Announces Successful SIRONA Trial Results, Demonstrating Sirolimus-Coated Balloon as a Promising Alternative for PAD Treatment
Devices Interventional
 HSMN NewsFeed - 14 Feb 2024
Efemoral Medical Granted Breakthrough Device Designation
Devices Interventional FDA
 HSMN NewsFeed - 14 Dec 2020
Efemoral Medical Announces Successful First-In-Human Use of the Efemoral(TM) Vascular Scaffold System
Devices Interventional
 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 - 26 Apr 2017
Mercator MedSystems Announces First Enrollment in the TANGO Trial for BTK Vascular Disease
Devices Interventional Drug Delivery
 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 - 30 Sep 2015
Intact Vascular Announces Conditional FDA Approval for Tack Optimized Balloon Angioplasty II (TOBA II) Study and Enrollment of First Patients
Devices Interventional FDA
 HSMN NewsFeed - 3 Aug 2015
CMS Approves Add-on Payment for Lutonix(R) Drug-Coated Balloon for Inpatient Use
Devices Interventional Reimbursement
 HSMN NewsFeed - 9 Jun 2015
CMS Further Improves Reimbursement for Lutonix DCB for Outpatient Use
Devices Interventional Reimbursement
 HSMN NewsFeed - 4 Sep 2014
EndoCross Receives CE Mark Approval for the ENABLER-C Coronary Catheter System for the Crossing of Coronary Chronic Total Occlusions
Devices INterventional Cardiology 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 - 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 - 11 Oct 2012
Cook Medical’s Zilver(R) PTX(R) Trial Shows Sustained Patency after Three Years
Devices Interventional
 HSMN NewsFeed - 13 Aug 2012
Cook Medical’s Ongoing Zilver(R) PTX(R) Trial Data Show Higher Freedom From Target Lesion Revascularization (TLR) Rates Compared to Angioplasty and Bare Metal Stenting After Three Years
Devices Interventional
 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 - 25 Jul 2011
First Patient Enrolled in Lutonix Drug-Coated Balloon Pivotal Trial
Devices Interventional
 HSMN NewsFeed - 22 Jul 2011
BIOTRONIK Vascular Enters U.S. with First Peripheral Stent Implant in BIOFLEX-I IDE Clinical Trial
Devices Interventional
 HSMN NewsFeed - 2 Jun 2011
NovoStent Announces Appointment of Rick Randall as Chairman of the Board
Devices Interventional Personnel
 HSMN NewsFeed - 12 May 2011
Avinger Receives CE Mark Approval for Its Wildcat Catheter for the Treatment of Peripheral Artery Chronic Total Occlusions and Will Present Results from Its Connect Study at EuroPCR Conference May 17-19
Devices Interventional Regulatory
 HSMN NewsFeed - 7 Apr 2011
Spectranetics to Initiate Landmark Randomized Study of Laser Treatment for Peripheral Artery Disease
Devices Interventional
 HSMN NewsFeed - 25 Feb 2011
Avinger Announces Expansion of Its Sales Force as the Company Plans for Growth in 2011
Devices Interventional
 HSMN NewsFeed - 2 Feb 2011
FSS Receives Full Investigational Device Exemption (IDE) Approval for its FlexStent(R) Stent System
Devices Interventional FDA
 HSMN NewsFeed - 11 Nov 2010
Flexible Stenting Solutions, Inc. Signs Distribution Agreement with Goodman Co. Ltd.
Devices Interventional Distribution
 HSMN NewsFeed - 4 Nov 2010
BIOTRONIK Announces First Patient Enrollment in the BIOLUX P-I Clinical Study Investigating Drug-Eluting Balloon Therapy for Peripheral Artery Disease
Devices Interventional
 HSMN NewsFeed - 21 Dec 2009
Gore Expands Line of GORE PROPATEN(R) Vascular Grafts
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 - 17 Mar 2009
Flexible Stenting Solutions, Inc. Announces IDE Submission for FlexStent(R) Femoropopliteal Self Expanding Stent System
Devices Interventional FDA
 HSMN NewsFeed - 3 Mar 2009
Flexible Stenting Solutions, Inc. Receives CE Mark for New FlexStent Biliary Self Expanding Stent System
Devices Interventional Regulatory
 HSMN NewsFeed - 11 Jun 2008
Interim Results for the Zilver(R) PTX(TM) Clinical Study from Cook Medical Show Promise for Improving the Treatment of Blockages in the Femoropopliteal Artery
Devices Interventional
 HSMN NewsFeed - 31 Mar 2008
NovoStent Announces Implantation of World's Longest Peripheral Stent
Devices Interventional
 HSMN NewsFeed - 11 Dec 2007
W. L. GORE & ASSOCIATES ANNOUNCES SUMMARY OF GORE PROPATEN VASCULAR GRAFT STUDY DATA PRESENTED AT 34TH ANNUAL VEITHSYMPOSIUM™
Devices Interventional
 HSMN NewsFeed - 30 Jan 2007
First International Trial of Drug-Eluting Peripheral Artery Stent Results Encouraging
Devices Interventional
 HSMN NewsFeed - 29 Jan 2007
FDA Grants Boston Scientific Clearance to Expand PolarCath(TM) Peripheral Dilatation System Offering with New Balloon Length
Devices Interventional FDA
 HSMN NewsFeed - 15 Nov 2006
FDA Clears GORE PROPATEN Vascular Graft
Devices FDA
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