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Searching News Database:  ASPIRE Study 

 HSMN NewsFeed - 29 Apr 2021
Cerapedics Announces FDA Breakthrough Device Designation Granted for P-15L Bone Graft for the Treatment of Degenerative Disc Disease
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 4 Jul 2016
European Commission Approves Extended Indication For Amgen's Kyprolis(R) (Carfilzomib) For The Treatment Of Relapsed Multiple Myeloma Patients
Biopharmaceuticals Oncology Regulatory
 HSMN NewsFeed - 29 Feb 2012
Study of Next Step Toward Artificial Pancreas from Medtronic Meets Efficacy Endpoints
Devices Endocrinology Drug Delivery Monitoring
 HSMN NewsFeed - 25 Jun 2010
Medtronic Begins Enrollment in ASPIRE Pivotal Study of Low Glucose Suspend Integrated System
Devices Endocrinology
 HSMN NewsFeed - 14 Nov 2006
Kensey Nash Announces Commencement of Carotid Pivotal Trial for TriActiv ProGuard 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 Apr 2006
Kensey Nash Announces Completion of Carotid Pilot Trial Using the TriActiv(R) ProGuard(TM) System
Devices Interventional
 HSMN NewsFeed - 23 Mar 2006
REMICADE(R) Is Approved in Australia for Treatment of Early Rheumatoid Arthritis and Psoriatic Arthritis
Biopharmaceuticals Regulatory
 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 - 12 Jan 2006
Kensey Nash Submits QuickCat(TM) Extraction Catheter 510(k) Application to FDA
Devices FDA
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ASPIRE Study
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