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News Industry News

Avinger Announces FDA Clearance and U.S. Launch of Breakthrough Treatment for Patients With Peripheral Artery Disease

March 01, 2016

News Industry News

Gore Launches New 7.5 cm Length GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface

February 29, 2016

News Daily News

Even Without Proof of Benefit, 1 in 6 Patients Still Given Vena Caval Filters

Yael L. Maxwell

February 29, 2016

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for February 2016

Shelley Wood

February 28, 2016

News Daily News

MitraClip Manufacturer Issues Safety Notice on Proper Deployment

Caitlin E. Cox

February 28, 2016

News Industry News

Endologix Announces First U.S. Commercial Implant of AFX®2 Bifurcated Endograft System

February 28, 2016

News Industry News

LivaNova PLC Receives Regulatory Approval in Japan for the Solo Smart Stentless Tissue Aortic Valve

February 28, 2016

News Conference News CRT 2016

Will the MitraClip and Other Gadgets Make Headway in Functional MR?

Shelley Wood

February 25, 2016

News Opinion Fellow Talk

Part of the Job: Handling Bad Outcomes in the Cath Lab

Luke Kohan, MD

February 24, 2016

News Industry News

Micell Technologies Highlights Data From Published Propensity Analysis of MiStent SES® and Market Standard Xience V® Coronary Stent

February 24, 2016

News Daily News

Transcatheter Aortic Valve Outcomes Better in Women Than Men at 12 Months

Shelley Wood

February 23, 2016

News Daily News

Increased Risk of Device Thrombosis With Bioresorbable Scaffold, but Some Say Risks Can Be Mitigated

Michael O'Riordan

February 23, 2016

News Conference News CRT 2016

Health Apps, Bar Codes, and Big Data: The “Brave New World” of Medical Device Innovation

Shelley Wood

February 23, 2016

News Daily News

PFO Closure Faces Renewed Scrutiny in Patient-Level Meta-Analysis

Yael L. Maxwell

February 22, 2016

Presentation

Device Closure of PFO After Stroke: Pooled Analysis of Completed Randomized Trials

Presenter: David M. Kent

February 22, 2016

News Industry News

Boston Scientific Receives U.S. FDA Approval For Quadripolar Leads And Initiates Global Trial To Expand MRI Labeling To The U.S. And Asia

February 22, 2016

News Conference News CRT 2016

Registry Behind TASTE Reopens Thrombus Aspiration Question With New Analysis of Stent Thrombosis

Shelley Wood

February 22, 2016

News Industry News

Mitralign Percutaneous Annuloplasty System Earns CE Mark Approval for Functional Mitral Regurgitation

February 21, 2016

News Industry News

Medtronic Receives FDA Approval for Expanded Indication Trial in Low-Risk Aortic Stenosis Patients

February 21, 2016

News Industry News

Medtronic Receives CE Mark for Full Line of Cardiac Resynchronization Therapy-Defibrillators Compatible with MRI Scans

February 21, 2016

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Avinger Announces FDA Clearance and U.S. Launch of Breakthrough Treatment for Patients With Peripheral Artery Disease

Gore Launches New 7.5 cm Length GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface

Even Without Proof of Benefit, 1 in 6 Patients Still Given Vena Caval Filters

TCTMD’s Top 10 Most Popular Stories for February 2016

MitraClip Manufacturer Issues Safety Notice on Proper Deployment

Endologix Announces First U.S. Commercial Implant of AFX®2 Bifurcated Endograft System

LivaNova PLC Receives Regulatory Approval in Japan for the Solo Smart Stentless Tissue Aortic Valve

Will the MitraClip and Other Gadgets Make Headway in Functional MR?

Part of the Job: Handling Bad Outcomes in the Cath Lab

Micell Technologies Highlights Data From Published Propensity Analysis of MiStent SES® and Market Standard Xience V® Coronary Stent

Transcatheter Aortic Valve Outcomes Better in Women Than Men at 12 Months

Increased Risk of Device Thrombosis With Bioresorbable Scaffold, but Some Say Risks Can Be Mitigated

Health Apps, Bar Codes, and Big Data: The “Brave New World” of Medical Device Innovation

PFO Closure Faces Renewed Scrutiny in Patient-Level Meta-Analysis

Device Closure of PFO After Stroke: Pooled Analysis of Completed Randomized Trials

Boston Scientific Receives U.S. FDA Approval For Quadripolar Leads And Initiates Global Trial To Expand MRI Labeling To The U.S. And Asia

Registry Behind TASTE Reopens Thrombus Aspiration Question With New Analysis of Stent Thrombosis

Mitralign Percutaneous Annuloplasty System Earns CE Mark Approval for Functional Mitral Regurgitation

Medtronic Receives FDA Approval for Expanded Indication Trial in Low-Risk Aortic Stenosis Patients

Medtronic Receives CE Mark for Full Line of Cardiac Resynchronization Therapy-Defibrillators Compatible with MRI Scans

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