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Bluegrass Vascular Secures CE Mark Approval and Announces Successful Commercial Use of The Surfacer® Inside-Out® Access Catheter System

August 30, 2016

News Industry News

Vasorum Ltd. Receives FDA Approval for Celt ACD® Vascular Closure Device

July 21, 2016

News Industry News

Essential Medical Inc. Announces CE Mark Approval for the MANTA™ Large Bore Vascular Closure Device

July 18, 2016

News Industry News

Essential Medical Inc. Announces FDA Approval to Begin a U.S. Clinical Trial for the MANTA™ Large Bore Vascular Closure Device

July 08, 2016

News Industry News

Endologix Completes Patient Enrollment in the Ovation® LIFE (Least Invasive Fast-Track EVAR) Study

May 17, 2016

News Industry News

St. Jude Medical Secures CE Mark Approval of MRI Compatibility for the Nanostim Leadless Pacemaker

March 09, 2016

News Industry News

Boston Scientific Receives CE Mark For Eluvia™ Drug-Eluting Vascular Stent and Announces Initiation of New Clinical Trial

February 21, 2016

News Industry News

Essential Medical Inc. Announces Successful Completion of EU Clinical Studies for MANTA™ Large Bore Vascular Closure Device

January 31, 2016

News Industry News

First Patients Enrolled in the Gore RELINE MAX Clinical Study

December 15, 2015

News Industry News

Medeon Biodesign Announces Successful First-in-man Studies for Large Bore Vascular Closure Device

November 02, 2015

News Industry News

Accessing the Heart Via the Arm During AD-HOC PCI has Similar Ischemic Outcomes Compared to Conventional Groin Access at One Year with Potential for Lower Bleeding

October 12, 2015

News Industry News

FDA Clears CorPath® System for Robotic-assisted Radial Access PCI Procedures

October 06, 2015

News Industry News

Medtronic's Valiant® Thoracic Stent Graft System Demonstrates Durability After Five Years

October 05, 2015

News Industry News

St. Jude Medical Gains CE Mark for 27mm & 29mm Portico TAVR Valves to Complete a Full Portfolio of Portico Sizing Options for Physicians Treating Patients with Aortic Stenosis

September 18, 2015

News Industry News

Proteon Therapeutics Announces Top-Line Results From Phase 1 Study of Investigational Drug Vonapanitase in Patients With Symptomatic Peripheral Artery Disease

August 14, 2015

News Industry News

Vascular Solutions Expands Launch of PolarCath(TM) System With 0.035” Catheters

August 03, 2015

News Industry News

Essential Medical Inc. Announces Successful Commencement of EU Studies for MANTA™ Large Bore Vascular Closure Device

July 27, 2015

News Industry News

Global Trial Finds Medtronic Micra® Transcatheter Pacemaker Meets Initial Safety Measures in Wide Range of Patients

May 14, 2015

News Industry News

Essential Medical Inc. Announces Successful Additional Clinical Studies For MANTA™ Large Bore Vascular Closure Device

May 04, 2015

News Industry News

Direct Flow Medical, Inc Announces FDA Approval to Broaden SALUS U.S. Pivotal Trial

April 09, 2015

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Bluegrass Vascular Secures CE Mark Approval and Announces Successful Commercial Use of The Surfacer® Inside-Out® Access Catheter System

Vasorum Ltd. Receives FDA Approval for Celt ACD® Vascular Closure Device

Essential Medical Inc. Announces CE Mark Approval for the MANTA™ Large Bore Vascular Closure Device

Essential Medical Inc. Announces FDA Approval to Begin a U.S. Clinical Trial for the MANTA™ Large Bore Vascular Closure Device

Endologix Completes Patient Enrollment in the Ovation® LIFE (Least Invasive Fast-Track EVAR) Study

St. Jude Medical Secures CE Mark Approval of MRI Compatibility for the Nanostim Leadless Pacemaker

Boston Scientific Receives CE Mark For Eluvia™ Drug-Eluting Vascular Stent and Announces Initiation of New Clinical Trial

Essential Medical Inc. Announces Successful Completion of EU Clinical Studies for MANTA™ Large Bore Vascular Closure Device

First Patients Enrolled in the Gore RELINE MAX Clinical Study

Medeon Biodesign Announces Successful First-in-man Studies for Large Bore Vascular Closure Device

Accessing the Heart Via the Arm During AD-HOC PCI has Similar Ischemic Outcomes Compared to Conventional Groin Access at One Year with Potential for Lower Bleeding

FDA Clears CorPath® System for Robotic-assisted Radial Access PCI Procedures

Medtronic's Valiant® Thoracic Stent Graft System Demonstrates Durability After Five Years

St. Jude Medical Gains CE Mark for 27mm & 29mm Portico TAVR Valves to Complete a Full Portfolio of Portico Sizing Options for Physicians Treating Patients with Aortic Stenosis

Proteon Therapeutics Announces Top-Line Results From Phase 1 Study of Investigational Drug Vonapanitase in Patients With Symptomatic Peripheral Artery Disease

Vascular Solutions Expands Launch of PolarCath(TM) System With 0.035” Catheters

Essential Medical Inc. Announces Successful Commencement of EU Studies for MANTA™ Large Bore Vascular Closure Device

Global Trial Finds Medtronic Micra® Transcatheter Pacemaker Meets Initial Safety Measures in Wide Range of Patients

Essential Medical Inc. Announces Successful Additional Clinical Studies For MANTA™ Large Bore Vascular Closure Device

Direct Flow Medical, Inc Announces FDA Approval to Broaden SALUS U.S. Pivotal Trial

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