Devices and methods for removal of acute blockages from blood vessels
US-2016015402-A1 · Jan 21, 2016 · US
US12016582B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12016582-B2 |
| Application number | US-202218053217-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 7, 2022 |
| Priority date | Jun 12, 2019 |
| Publication date | Jun 25, 2024 |
| Grant date | Jun 25, 2024 |
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Official abstract text for this publication.
Retrieval of material from vessel lumens can be improved by use of a distal element comprising an expandable mesh. a treatment device includes an elongated member having a proximal portion and a distal portion configured to be positioned within a blood vessel at a treatment site at or near a thrombus. A distal element comprising an expandable mesh is coupled to the distal portion of the elongated member via a connection assembly. In an expanded state, at least a portion of the mesh is configured to be in apposition with the blood vessel wall at the treatment site to anchor or stabilize the elongated member with respect to the blood vessel. The distal element can be electrically coupled to an extracorporeal current generator.
Opening claim text (preview).
The invention claimed is: 1. A treatment device, comprising: a guidewire having a proximal portion and a distal portion configured to be positioned within a blood vessel at a treatment site at or near a thrombus; and a distal element having a proximal end portion and a distal end portion, the proximal end portion directly coupled to the distal portion of the guidewire via a connection assembly and the distal end portion comprising a curved distal end surface, wherein the distal end portion is unattached to the guidewire such that the distal end portion can move freely with respect to the guidewire, and wherein the distal element has a constrained state for delivery to the treatment site and an expanded state, wherein the guidewire extends through at least a portion of a cavity of the distal element, and wherein the distal element is configured to rotate about the guidewire, wherein, in the expanded state, the distal element is configured to expand into contact with the blood vessel wall at the treatment site. 2. The treatment device of claim 1 , wherein the guidewire extends through an entire length of the distal element. 3. The treatment device of claim 1 , wherein the guidewire comprises an elongated tubular element having a lumen extending therethrough. 4. The treatment device of claim 3 , wherein the elongated tubular element is a hypotube. 5. The treatment device of claim 3 , wherein a distal portion of the elongated tubular element is joined to a proximal portion of the connection assembly. 6. The treatment device of claim 1 , further comprising a coil positioned around a region of the guidewire that is proximal to the connection assembly. 7. The treatment device of claim 1 , further comprising a coil positioned around a region of the guidewire that is distal to the connection assembly. 8. The treatment device of claim 1 , wherein the distal element comprises a plurality of filaments. 9. The treatment device of claim 8 , wherein each of the filaments has a first end and a second end opposite the first end, and wherein both the first and second ends of the filaments are fixed relative to one another at the connection assembly. 10. The treatment device of claim 8 , wherein each of the filaments terminate at only one end of the distal element. 11. The treatment device of claim 10 , wherein the filaments form an opening at an end of the distal element opposite the only one end. 12. The treatment device of claim 1 , wherein the distal element has a globular shape. 13. The treatment device of claim 1 , wherein the distal element has a central portion between the proximal and distal end portions, and wherein the distal element has a greater radial dimension along the central portion than along the proximal and distal portions. 14. A treatment device, comprising: a guidewire having a proximal portion and a distal portion configured to be positioned within a blood vessel at a treatment site at or near a thrombus; and a distal element having a proximal region, a distal region, and a cavity through which the guidewire is positioned, wherein the proximal region is directly coupled to the distal portion of the guidewire via a connection assembly and the distal region is unattached to the guidewire such that the distal region can move freely with respect to the guidewire, and wherein the distal element is configured to rotate about the guidewire, wherein the distal element has a constrained state for delivery to the treatment site and an expanded state, wherein the distal element extends distally and radially inwardly along the distal region towards a distal terminus of the distal element, and wherein, in the expanded state, the distal element is configured to expand into contact with the blood vessel wall at the treatment site. 15. The treatment device of claim 14 , wherein the guidewire extends through an entire length of the distal element. 16. The treatment device of claim 14 , wherein the distal element has a globular shape. 17. The treatment device of claim 14 , wherein the distal element comprises a plurality of filaments. 18. The treatment device of claim 17 , wherein each of the filaments has a first end and a second end opposite the first end, and wherein both the first and second ends of the filaments are fixed relative to one another at the connection assembly. 19. The treatment device of claim 14 , wherein the guidewire comprises an elongated tubular element having a lumen extending therethrough. 20. The treatment device of claim 19 , wherein a distal portion of the elongated tubular element is joined to a proximal portion of the connection assembly.
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