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InterStim™ Micro Neurostimulator and InterStim™ SureScan™ MRI Leads Receive FDA Approval

LINQ II Insertable Cardiac Monitor Receives FDA Clearance and CE Mark

Medtronic Introduces MiniMed™ Mio™ Advance Infusion Set Enabling Fewer Insertion Steps for People with Diabetes in the U.S.

Percept PC Deep Brain Stimulation System with BrainSense Technology Receives FDA Approval

Medtronic Evolut TAVI System Receives Expanded Indication in Europe to Treat Severe Aortic Stenosis Patients at Low Risk for Surgical Mortality

ABRE Clinical Study Meets Primary Safety and Effectiveness Endpoints

Medtronic Micra™ AV Receives CE Mark

MiniMed 780G Advanced Hybrid Closed Loop System Designed to Further Simplify Type 1 Diabetes Management Receives CE Mark

Medtronic Resolute Onyx DES Receives First and Only One-Month DAPT Indication for High Bleeding Risk Patients in Europe

New Directional Cannula Provides More Flexibility and Control to Balloon Kyphoplasty Procedures

New Directional Cannula Provides More Flexibility and Control to Balloon Kyphoplasty Procedures

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