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Aug 6, 2010

Medtronic Completes Enrollment in Clinical Study of Complete SE(R) (Self-Expanding) Vascular Stent

Milestone Shows Progress on Indication-Specific Trials for Treating Peripheral Arterial Disease

MINNEAPOLIS, Aug 06, 2010 (BUSINESS WIRE) -- With an expanded focus on addressing peripheral arterial disease (PAD), Medtronic, Inc. (NYSE: MDT), today announced that it has completed enrollment...
Aug 5, 2010

First Patient Treated with Medtronic's Valiant(R) Thoracic Stent Graft in Aortic Dissection Trial

Minimally Invasive Procedure May Stabilize Bleeding and Improve Clinical Outcomes

MINNEAPOLIS, Aug 05, 2010 (BUSINESS WIRE) -- Marking a major milestone toward expanding the use and utility of minimally invasive endovascular procedures, Medtronic, Inc. (NYSE: MDT), today...
Jul 29, 2010

Medtronic Launches Novel Clinical Trial Evaluating Spinal Cord Stimulation Therapy for Heart Failure

Defeat-HF Trial Aims to Slow HF Progression with Neurostimulation

MINNEAPOLIS, Jul 29, 2010 (BUSINESS WIRE) -- Medtronic, Inc. (NYSE: MDT) today announced the global launch of the Defeat-HF (Determining the Feasibility of Spinal Cord Neuromodulation for the...
Jul 27, 2010

Study Shows Practice Improvement Program Enhances Guideline-Recommended Device and Drug Therapy Use for Heart Failure Patients

IMPROVE HFStudy Published in Circulation Demonstrates Improved Adherence to Five of Seven Guideline-Recommended Care Measures

MINNEAPOLIS, Jul 26, 2010 (BUSINESS WIRE) -- Results of the largest U.S. outpatient heart failure clinical study show that implementation of a process improvement program significantly improved...
Jul 27, 2010

Medtronic's AMPLIFY(TM) rhBMP-2 Matrix Receives Positive Votes from FDA Advisory Panel on All Three Key Questions: Safety, Effectiveness and Benefit/Risk

New biologic bone graft product demonstrated superior fusion rates compared to current standard of care for complex fusion procedures of the lower spine in the pivotal clinical trial

MINNEAPOLIS, Jul 27, 2010 (BUSINESS WIRE) -- The U.S. Food and Drug Administration (FDA) Orthopaedic and Rehabilitation Devices Panel today voted 9 for and 4 against (1 abstention) on safety and...

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