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Searching News Database:  TriActiv FX 

 HSMN NewsFeed - 14 Nov 2006
Kensey Nash Announces Commencement of Carotid Pivotal Trial for TriActiv ProGuard System
Devices Interventional
 HSMN NewsFeed - 23 Oct 2006
Kensey Nash Receives CE Mark Approval for New ThromCat(TM) Thrombectomy Catheter System
Devices Interventional
 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 May 2006
Kensey Nash Announces Acquisition of Assets of IntraLuminal Therapeutics, Inc.
Devices Interventional Cardiology Mergers & Acquisitions
 HSMN NewsFeed - 27 Apr 2006
Kensey Nash Receives FDA 510(k) Clearance for New ThromCat(TM) Thrombectomy Catheter System
Devices 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 - 10 Mar 2006
Kensey Nash Receives FDA 510(k) Clearance for QuickCat(TM) Extraction Catheter
Devices Interventional FDA
 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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