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FDA Approves Edwards EVOQUE® Tricuspid Valve Replacement System | Knobbe Martens

The U.S. Food and Drug Administration (“FDA”) recently approved the Edwards EVOQUE® Tricuspid Valve Replacement System (the “EVOQUE® system”) for use in treating Tricuspid.

United statesKnobbe martensEdwards lifesciencesDrug administrationTricuspid valve replacement systemTricuspid regurgitationInstructions forPatient guideDaveen chopraData analysis plan vennFull cohortBreakthrough pathway cohortMedi tech insightsGlobal tricuspid valve repair marketNorth america

BIOSOLVE-IV Full-Cohort Two-Year Data Confirm Excellent Safety and Efficacy Profile of Magmaris Resorbable Magnesium Scaffold

Magmaris Scaffold Performs Well in Real World Settings Even in More Complex Patient Groups

Region flamandeJohan bennettLukaskrankenhaus neussInterventionalist at university hospitals leuvenTranscatheter cardiovascular therapeuticsMagmaris resorbable magnesium scaffoldCoronary interventionalistUniversity hospitals leuvenPresident vascular interventionResorbable magnesium scaffoldReal world settingFull cohortReal world setting primarySecondary endpoint analysisCardiovascular interventionsDegradation kinetics

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