Occlusive medical device with sealing member
US-2024423599-A1 · Dec 26, 2024 · US
US9301827B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9301827-B2 |
| Application number | US-201414171088-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 3, 2014 |
| Priority date | Jun 3, 2011 |
| Publication date | Apr 5, 2016 |
| Grant date | Apr 5, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A parent artery occlusion (PAO) device which provides for immediate occlusion of a cerebral artery to isolate a defect. The PAO device includes a self-expanding wire-frame prolate structure which is partially covered with an ePTFE membrane.
Opening claim text (preview).
We claim: 1. An embolic implant, said embolic implant characterized by a proximal end and a distal end, said embolic implant comprising: a wire frame structure characterized by a proximal end and a distal end, said wire-frame structure comprising: a pair of opposing zigzag segments including a plurality of V-shaped elements defining an open end, the V-shaped elements joined at the open end of the V-shaped elements via short longitudinally aligned struts to form a central portion of the wire-frame structure, said short struts being longitudinally displaced from each other, said V-shaped elements defining proximal or distal vertices pointing proximally or distally away from the center of the wire frame structure; a first plurality of longitudinally oriented struts extending from the proximally pointing vertices of the V-shaped elements, said longitudinally oriented struts being joined together near the radial center of the wireframe structure at the proximal end of the embolic implant; a second plurality of longitudinally oriented struts extending from the distally pointing vertices of the V-shaped elements, said longitudinally oriented struts being joined together near the radial center of the wireframe structure at the distal end of the embolic implant; wherein the wireframe structure is formed of a self-expanding material; a detachment joint fixed to the proximal end of the embolic implant; and a blood impermeable membrane disposed over the proximal end of the embolic implant, said blood impermeable membrane extending over at least one of the zigzag segments. 2. The embolic implant of claim 1 wherein the wire-frame structure further comprises a pseudoelastic metal alloy. 3. The embolic implant of claim 1 wherein the membrane comprises ePTFE impregnated with an adhesive, said membrane being glued to the wire-frame structure. 4. The embolic implant of claim 1 wherein the membrane comprises two layers of ePTFE impregnated with an adhesive, said membrane being glued to the wire-frame structure. 5. The embolic implant of claim 1 wherein the wire frame structure has a fully expanded configuration with a diameter of about 5 mm, and a second fully compacted configuration with a diameter of less than about 1 mm. 6. The system of claim 1 wherein the wire frame structure has a fully expanded configuration with a diameter of about 5 mm, and a second fully compacted configuration with a diameter of less than about 0.6 mm. 7. A system for occlusion of an artery, said system comprising: an embolic implant characterized by a proximal end and a distal end, said embolic implant comprising: a wire frame structure characterized by a proximal end and a distal end, said wire-frame structure comprising: a pair of opposing zigzag segments including a plurality of V-shaped elements defining an open end, the V-shaped elements joined at the open end of the V-shaped elements via short longitudinally aligned struts to form a central portion of the wire-frame structure, said short struts being longitudinally displaced from each other, said V-shaped elements defining proximal or distal vertices pointing proximally or distally away from the center of the wire frame structure; a first plurality of longitudinally oriented struts extending from the proximally pointing vertices of the V-shaped elements, said longitudinally oriented struts being joined together near the radial center of the wireframe structure at the proximal end of the embolic implant; a second plurality of longitudinally oriented struts extending from the distally pointing vertices of the V-shaped elements, said longitudinally oriented struts being joined together near the radial center of the wireframe structure at the distal end of the embolic implant; wherein the wireframe structure is formed of a self-expanding material; an electrolytic detachment joint fixed to the proximal end of the embolic implant; and a blood impermeable membrane disposed over the proximal end of the embolic implant, said blood impermeable membrane extending over at least one of the zigzag segments; a delivery catheter adapted for navigation through the patient's vasculature to the parent artery, said delivery catheter also adapted to house the embolic implant within the distal tip of the delivery catheter; a deliver rod slidably disposed within the delivery catheter, said delivery rod having a distal end fixed to the embolic implant via the electrolytic detachment joint; and a conductor for supplying power to the electrolytic detachment joint from a power supply. 8. The system of claim 7 wherein the wire-frame structure further comprises a pseudoelastic metal alloy. 9. The system of claim 7 wherein the membrane comprises ePTFE impregnated with an adhesive, said membrane being glued to the wire-frame structure. 10. The system of claim 7 wherein the membrane comprises two layers of ePTFE impregnated with an adhesive, said membrane being glued to the wire-frame structure. 11. The system of claim 7 wherein the wire frame structure has a fully expanded configuration with a diameter of about 5 mm, and a second fully compacted configuration with a diameter of less than about 1 mm. 12. The system of claim 7 wherein the wire frame structure has a fully expanded configuration with a diameter of about 5 mm, and a second fully compacted configuration with a diameter of less than about 0.6 mm. 13. An embolic implant, said embolic implant characterized by a proximal end and a distal end, said embolic implant comprising: a wire frame structure characterized by a proximal end and a distal end, said wire-frame structure comprising: a pair of opposing zigzag segments including a plurality of V-shaped elements defining an open end, the V-shaped elements joined at the open end of the V-shaped elements via short longitudinally aligned struts to form a central portion of the wire-frame structure, said short struts being longitudinally displaced from each other, said V-shaped elements defining proximal or distal vertices pointing proximally or distally away from the center of the wire frame structure; a plurality of longitudinally oriented struts extending from the proximally pointing vertices of the V-shaped elements, said longitudinally oriented struts being joined together near the radial center of the wire-frame structure at the proximal end of the embolic implant; wherein the wireframe structure is formed of a self-expanding material; a detachment joint fixed to the proximal end of the embolic implant; and a membrane disposed over the proximal end of the embolic implant, said membrane having a proximal facing surface, said membrane being impermeable to blood on the proximal facing surface such that blood is substantially prevented from flowing through the implant when deployed in the parent artery. 14. The embolic implant of claim 13 wherein the wire-frame structure further comprises a pseudoelastic metal alloy. 15. The embolic implant of claim 13 wherein the membrane comprises ePTFE impregnated with an adhesive, said membrane being glued to the wire-frame structure. 16. The embolic implant of claim 13 wherein the membrane comprises two layers of ePTFE impregnated with an adhesive, said membrane being glued to the wire-frame structure. 17. The embolic implant of claim 13 wherein the wire frame structure has a fully expanded configuration with a diameter of about 5 mm, and a second fully compacted configuration with a diameter of less than about 1 mm. 18. The system of claim 13 wherein the wire frame structure has a fully expa
Porous materials, e.g. foams or sponges · CPC title
Macromolecular materials · CPC title
Adhesives for ostomy devices · CPC title
partial occlusion · CPC title
Methods of manufacturing · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.