Septal defect occlusion device
AssigneeEdwards Lifesciences Corporation
InventorsJohn J. Desrosiers, Nima V. Nia, Biswa P. Das, Sandip Vasant Pawar, Juan Valle Raleigh
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AssigneeEdwards Lifesciences Corporation
InventorsJohn J. Desrosiers, Nima V. Nia, Biswa P. Das, Sandip Vasant Pawar, Juan Valle Raleigh
Estimating the term…
An implantable device can be configured to occlude an opening in a septum of a heart, such as a perimembranous ventricular septal defect. The device can comprise an expandable member expandable from a first state to a second state upon contact with a fluid. The implantable device in the second state can be configured to occlude the opening in the septum, thereby preventing blood from leaking through the opening and across the septum. The implantable device can be substantially or completely devoid of metal, resulting in a reduced likelihood that the implantable device affects the function of heart valves near the opening of the septum or leads to tissue erosion.
An implantable device for occluding an opening in a septum of a heart comprising an expandable member configured to expand from a first state to an expanded second state upon contact with fluid, the expandable member having a first end portion, an intermediate portion, and a second end portion arranged along a longitudinal axis extending through the expandable member, wherein the intermediate portion is disposed between the first end portion and the second end portion, wherein the expandable member is asymmetrical with respect to a transverse axis that extends through the intermediate portion and is perpendicular to the longitudinal axis with the first end portion having a smaller cross-sectional area in a plane perpendicular to the longitudinal axis than the second end portion when the expandable member is in the expanded second state.
An implantable medical device for occluding an opening of a ventricular septal defect of a heart comprising:
A method of implanting a medical device in a septum of a heart, the medical device comprising first and second end portions and an intermediate portion between the first and second end portions, wherein the first end portion, the intermediate portion, and the second end portion are arranged along a longitudinal axis of the medical device, the method comprising:
Dependencies are inferred from the claim text.