Vascular filter having articulation region and methods of use in the ascending aorta
First Claim
1. An apparatus for filtering emboli comprising:
- an elongated member having a distal region;
a support hoop attached to the distal region, the support hoop having an articulation region;
a blood permeable sac affixed to the support hoop; and
a delivery sheath having a lumen extending therethrough and further including a distal cavity therein configured to receive the elongated member, support hoop and blood permeable sac in a contracted state, the sheath having a window disposed proximally of the cavity, the window being sized and configured such that the support structure expands through the window to engage an interior wall of a patient'"'"'s vessel when the apparatus is in a deployed state.
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Accused Products
Abstract
Apparatus and methods are provided for use in filtering emboli from a vessel such as the ascending aorta, wherein a vascular device comprises a support hoop having an articulation region connected near a distal end of an elongated member, a blood permeable sac affixed to the support hoop so that the support hoop forms a mouth of the blood permeable sac, a guide wire, and a delivery sheath. The articulation region comprises a reduced thickness region of the support hoop that prevents kinks from forming in the support hoop when the apparatus is contracted to its delivery state, and curved regions that close the mouth of the sac to prevent material escaping from the sac when the apparatus is collapsed for removal.
94 Citations
7 Claims
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1. An apparatus for filtering emboli comprising:
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an elongated member having a distal region; a support hoop attached to the distal region, the support hoop having an articulation region; a blood permeable sac affixed to the support hoop; and a delivery sheath having a lumen extending therethrough and further including a distal cavity therein configured to receive the elongated member, support hoop and blood permeable sac in a contracted state, the sheath having a window disposed proximally of the cavity, the window being sized and configured such that the support structure expands through the window to engage an interior wall of a patient'"'"'s vessel when the apparatus is in a deployed state. - View Dependent Claims (2, 3, 4, 5, 6, 7)
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Specification