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Searching News Database:  saphenous vein graft 

 HSMN NewsFeed - 11 Jan 2021
Marizyme Announces the Use of DuraGraft(R) as the Standard-of-Care in Patients Undergoing Coronary Artery Bypass Surgery (CABG) at Vienna Heart Center North Floridsdorf
Devices Cardiology
 HSMN NewsFeed - 23 Feb 2018
Vascular Graft Solutions: External Stenting of Vein Grafts is Associated With High Early Patency Rates
Devices Cardiology
 HSMN NewsFeed - 25 May 2012
Medtronic Resolute(R) Stent Shows Strong Performance in Heart Disease Patients With and Without Diabetes
Devices Interventional Cardiology Endocrinology
 HSMN NewsFeed - 10 Jan 2012
Interwest Partners Expands Medical Devices Team
Devices Venture Capital Personnel
 HSMN NewsFeed - 1 Dec 2011
Covidien's Embolic Protection Device Receives FDA Clearance
Devices Interventional FDA
 HSMN NewsFeed - 10 Jun 2011
MAQUET Cardiovascular Initiates Trial Comparing Use of MAQUET Pressure Controlling Syringe to Standard Syringe in Endoscopic Vessel Harvesting
Devices Cardiology
 HSMN NewsFeed - 18 May 2011
Medtronic Resolute(R) Drug-Eluting Stent Offers Strong Performance in Diabetic Patients with Heart Disease
Devices Interventional Cardiology
 HSMN NewsFeed - 12 Aug 2009
Nfocus Neuromedical Obtains CE Approval for New Vascular Reconstruction Device
Devices Interventional Regulatory
 HSMN NewsFeed - 9 Jul 2009
MAQUET Cardiovascular Awarded New Contract by Novation
Devices Cardiology Group Purchasing
 HSMN NewsFeed - 15 May 2009
Boston Scientific Announces Schedule for EuroPCR 2009
Devices Interventional Cardiology
 HSMN NewsFeed - 28 Apr 2009
FDA has Granted HUD (Humanitarian Use Device) Designation to ITGI's Pericardium Covered Stents, Over and Under(R) and Aneugraft(R), for Treatment of Perforations and Dissections of Native Coronary Arteries and Saphenous Vein Grafts
Devices Interventional Cardiology FDA
 HSMN NewsFeed - 1 Sep 2008
Biosensors DES Demonstrates Equivalent Safety and Efficacy to Industry Leading DES in First 'Real World, All Comers' Clinical Study
Devices Interventional Cardiology
 HSMN NewsFeed - 2 Jun 2008
Over and Under(R) Pericardium Covered Stent is now in use in England and Proves Great Deliverability
Devices Interventional Cardiology
 HSMN NewsFeed - 20 May 2008
ITGI Medical Launches Over and Under(R) Pericardium Covered Stent in England, Switzerland and Ireland
Devices Interventional Cardiology
 HSMN NewsFeed - 19 May 2008
Boston Scientific Announces Launch of Expanded Size Range of FilterWire EZ(TM) Embolic Protection System
Devices Interventional
 HSMN NewsFeed - 19 May 2008
ITGI Medical Launches Over and Under(R) Pericardium Covered Stent in England, Switzerland and Ireland
Devices Interventional Cardiology
 HSMN NewsFeed - 17 Apr 2008
Medtronic Announces CE Mark and European Launch of New 'Defender' Embolic Protection Filter
Devices Interventional Regulatory
 HSMN NewsFeed - 29 Mar 2008
Real-World Data from ARRIVE Registries Show Favorable Outcomes for TAXUS(R) Express(TM) Stent
Devices Interventional Cardiology
 HSMN NewsFeed - 12 Feb 2008
Nfocus Neuromedical Receives CE Mark for the CardioVasc(TM) Stent-Graft and Delivery System
Devices Interventional Cardiology Regulatory
 HSMN NewsFeed - 23 Oct 2007
Medtronic Trials Confirm Ability of Interceptor(R) Coronary Filter System and Export(R) Aspiration Catheter to Reduce Major Cardiac Events
Devices Interventional Cardiology
 HSMN NewsFeed - 25 Jul 2007
St. Jude Medical Announces FDA Clearance of the Proxis Embolic Protection System
Devices Interventional Cardiology FDA
 HSMN NewsFeed - 10 Jul 2007
Kensey Nash to Exit Embolic Protection Markets
Devices Interventional
 HSMN NewsFeed - 10 Apr 2007
Kensey Nash Receives Expanded CE Mark Approval for TriActiv(R) ProGuard(TM) Embolic Protection System in Carotid Anatomy
Devices Interventional Regulatory
 HSMN NewsFeed - 3 Apr 2007
ev3 Inc. and Volcano Corporation Announce Joint Marketing and Distribution Agreement
Devices Interventional Distribution
 HSMN NewsFeed - 24 Jan 2007
ev3 Inc. Announces US FDA Approval of PROTEGE(R) RX Carotid Stent
Devices Interventional FDA
 HSMN NewsFeed - 8 Jan 2007
ev3 Inc. and FoxHollow Technologies, Inc. Announce a Clinical Collaboration and Distribution Agreement for SpideRX(R) and RockHawk(R) Technologies
Devices Interventional Distribution
 HSMN NewsFeed - 14 Dec 2006
FilterWire EZ(TM) Embolic Protection System Cleared By FDA For Carotid Artery Stenting
Devices Interventional FDA
 HSMN NewsFeed - 30 Nov 2006
Anesiva and Lumen Therapeutics Enter Agreement Granting Lumen Access to Data From Studies in Bypass Procedures
Biopharmaceuticals Cardiology Licensing
 HSMN NewsFeed - 14 Nov 2006
Kensey Nash Announces Commencement of Carotid Pivotal Trial for TriActiv ProGuard System
Devices Interventional
 HSMN NewsFeed - 18 Oct 2006
AVI BioPharma Initiates NEUGENE Antisense Clinical Program in Coronary Artery Bypass Grafting
Biopharmaceuticals Cardiology
 HSMN NewsFeed - 12 Jul 2006
Kensey Nash Receives FDA 510(k) Clearance for TriActiv FX(R) Embolic Protection System
Devices Interventional Cardiology FDA
 HSMN NewsFeed - 26 Jun 2006
ev3 Receives FDA Clearance for SpideRX(TM) Embolic Protection Device for Saphenous Vein Graft Angioplasty
Devices Interventional FDA
 HSMN NewsFeed - 26 Apr 2006
Kensey Nash Announces Completion of Carotid Pilot Trial Using the TriActiv(R) ProGuard(TM) System
Devices Interventional
 HSMN NewsFeed - 7 Mar 2006
Kensey Nash Announces Low 3.2% MACE Rate Achieved Using New TriActiv FX(R) Embolic Protection System
Devices Interventional Cardiology
 HSMN NewsFeed - 15 Feb 2006
Kensey Nash Receives CE Mark Approval for New TriActiv(R) ProGuard(TM) Embolic Protection System
Devices Interventional Cardiology Regulatory
 HSMN NewsFeed - 23 Jan 2006
Kensey Nash Submits TriActiv FX(R) Embolic Protection System 510(k) Application to FDA
Devices Interventional FDA
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