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331 results about "Iliac Aneurysm" patented technology

Abnormal balloon- or sac-like dilatation in the wall of any one of the iliac arteries including the common, the internal, or the external ILIAC ARTERY.

Bag for use in the intravascular treatment of saccular aneurysms

A bag for use in the intravascular treatment of saccular aneurysms and a method of forming the bag are disclosed. The bag is formed from a plurality of flexible, resilient filamentary members braided into a tubular sleeve and biased into a first shape having an expanded first diameter sized to substantially fill the aneurysm. The bag is resiliently deformable into a second shape having a diameter smaller than the first and sized to slidingly interfit within the lumen of a catheter. An opening is provided in the bag to receive a clotting medium, such as a platinum wire, on which blood clots can be induced to form by mechanical or electrolytic means. A closure is provided by biasing the filamentary members to form a constriction around the opening. In use the, bag is inserted into a saccular aneurysm via the catheter and expands to its first diameter upon release therefrom. Interstices between the interbraided filamentary members provide pores allowing blood from the aneurysm to enter the bag when the bag is positioned within the aneurysm. The clotting medium wire is packed into the bag, blood clots on the wire and occludes the aneurysm, sealing it off from the blood stream and preventing rupture. The wire is released from the catheter and is contained within the bag in the aneurysm.
Owner:PRODESCO

Aneurysm Occlusion Devices

InactiveUS20080281350A1Promote endothelial growthEliminate riskDilatorsCatheterMedicineImplanted device
An implantable occlusion device for bridging the neck of an aneurysm comprises a biocompatible matrix. The device is movable between a compressed position prior to implantation and a generally concave or cup-shaped position following implantation. The device may comprise a frame having a plurality of elements. The frame elements have a first pre-deployment position generally parallel to a major axis of the delivery lumen, and a second post-deployment position spread radially from the major axis of the delivery lumen. The biocompatible matrix and / or the frame elements may also form or be manipulated to form a generally concave or cupped shape. The matrix can be porous or semiporous, such as a foam or a reticulated matrix. The occlusion device can be folded, twisted and / or stretched to adopt a narrow profile for loading into a coaxial delivery device and expand in place as it adopts its original shape on release. The device may be released or manipulated to a desired shape to occlude an aneurysm. Methods of using the implantable device are also provided.
Owner:BIOMERIX CORP

Embolic balloon

An embolic balloon assembly is disclosed herein. The assembly includes a detachable balloon system which expands while aspirating a quantity of surrounding blood to occlude a vessel or aneurysm. The balloon has a distensible membrane having a plurality of orifices throughout its surface. Within the distensible membrane is a plurality of expandable members made from a shape memory alloy, e.g., Ni—Ti alloy, which expand upon application of a stimulus. Alternatively, the expandable members or a single expandable wire may be inserted separately into the distensible membrane. Once the balloon begins to expand, internal pressure within a volume defined by the distensible membrane begins to drop, forcing the device to aspirate a quantity of surrounding blood inside the volume which then begins to coagulate by stasis or some stimulus. The balloon may be configured to automatically release into the aneurysm or vessel or it may be released by a detachable joint.
Owner:SAADAT VAHID

Stitched stent grafts and methods for their fabrication

The present invention provides modular intraluminal tubular prostheses, particularly stents and stent-grafts, for the treatment of disease conditions, particularly aneurysms. Modular sections of the prostheses, or "prosthetic modules," may be selectively combined to form a composite prosthesis having characteristics which are tailored to the specific requirements of the patient. Each prosthetic module preferably includes one or more standard interface ends for engaging another module, the module / module interface typically comprising ends which overlap and / or lock within a predetermined axial range. Advantageously, the axial length, cross-section, perimeter, resilient expansive force, axial flexibility, liner permeability, liner extensibility, radial conformability, liner / tubal wall sealing and anchoring, and other prosthetic characteristics may be varied along the axis of the composite prosthesis, and also along the axis of each prosthetic module. The modules are preferably individually introduced into a lumen system of a patient body so that the composite prosthesis is assembled in situ. Ideally, selection of appropriate prosthetic modules and the flexibility of the interface overlap range provides a custom fit intraluminal prosthesis which provides a therapy tailored to the individual patient's needs.
Owner:MEDTRONIC AVE

Intravascular stent device

A very small diameter intravascular stent device which may be used to occlude or partially occlude an aneurysm in the human brain which is comprised of a thin-walled skeletal cylindrical tube formed of undulating or sinusoidal elements which, when compressed, nest tightly with each other.
Owner:CODMAN & SHURTLEFF INC

Tapered endovascular stent graft and method of treating abdominal aortic aneurysms and distal iliac aneurysms

An endovascular stent graft is provided for use in treating abdominal aortic aneurysms. The endovascular stent has a tapered section which allows it to accommodate markedly large aortas such as the abdominal aorta and still connects to standard modular aortic stent grafts. Methods of utilizing the stent to treat abdominal aortic aneurysms and distal iliac aneurysms are also provided.
Owner:COOK MEDICAL TECH LLC

Endovascular thin film devices and methods for treating and preventing stroke

InactiveUS20030060782A1Safely and permanently excludingPreventing initial or recurrent aneurysmal subarachnoid hemorrhageStentsCatheterIn situ polymerizationProsthesis
Devices for excluding aneurysms and treating atherosclerotic disease, for intra-aneurysmal occlusion; and devices for preventing distal emboli. The devices are generally pliable and collapsible thin film devices which can be delivered via a microcatheter into the desired location where they are deployed and undergo either a shape memory phase transformation or in situ polymerization to assume the stable configuration of a permanent endoluminal prosthesis. Prior to being caused to assume their final shape, the devices remain soft, collapsible and pliable to ensure atraumatic delivery through the vascular system. Upon reaching the endoluminal defect in the vessel, the device is extruded from the microcatheter. Devices are also provided for retrieving clots.
Owner:NEW YORK UNIV

Stent vascular intervention device and methods for treating aneurysms

InactiveUS20070021816A1Shorten the construction periodGreat effect on aneurysmal blood flowStentsBlood vesselsPorosityInsertion stent
The present invention relates to a stent including a variable porosity, tubular structure having pores defined by structural surfaces. The tubular structure has a low porosity region in proximity to or at either end of the tubular structure, where the low porosity region is less porous than other regions located on the tubular structure and fully or partially obstructs passage of fluid. Any arcuate path that starts at one point within the low porosity region and goes around the perimeter of the tubular structure to stop at the same point within the low porosity region must have at least a portion that is outside of the low porosity region. Also disclosed is a method of modifying blood flow within and near an opening of an aneurysm in a blood vessel by deploying one or more stents of the present invention near an opening of the aneurysm in a blood vessel.
Owner:THE RES FOUND OF STATE UNIV OF NEW YORK

Removable occlusion system for aneurysm neck

A system for treating an aneurysm in a vessel includes a delivery device having a delivery portion suitable for delivery of embolic material. The delivery device is placed in a neck of the aneurysm and an expandable member is placed proximate the neck. The expandable member is expanded to overlie substantially the entire neck. Embolic material is delivered to the aneurysm with a delivery device. The expandable member is held over the neck to inhibit movement of the embolic material out of the aneurysm. Blood is allowed to flow out of the aneurysm, past the neck of the aneurysm, and through the vessel while the expandable member is held over the neck of the aneurysm.
Owner:STRYKER CORP +1

Device forming an endoluminal intracorporeal endoprosthesis, in particular for the abdominal aorta

The invention relates to a device forming an endoluminal endoprosthesis. The device comprises at least a first segment, and upstream from said segment, at a predetermined distance therefrom, it comprises a "fixing" upstream segment made of a biocompatible material so as to be deployable from a closed or non-deployed position for insertion purposes to a deployed working position, the deployed working position being designed to be located in a healthy zone of blood vessel and being separated from the first segment by a predetermined distance defined by links of predetermined length. The invention makes it easy to recatheterize a blood vessel such as the abdominal aorta suffering from an aneurysm.
Owner:LEGONA ANSTALT

Detachable aneurysm neck closure patch

InactiveUS7128736B1Ear treatmentDilatorsClosure patchAneurysm neck
This is a device for bridging the neck of either an aneurysm in the vasculature and stabilizing the presence of vaso-occlusive devices (such as helically wound coils) in that aneurysm. The closure patch may be delivered either from the exterior of the distal end of a catheter or delivered from the catheter lumen. It is preferably implanted by the severance of an included electrolytically severable joint. The retainer assembly itself typically has a number of radially projecting elements which are, in turn, attached to a scrim-like fabric, preferably collagen-coated Dacron, extending among the various radially projecting elements. The closure patch is intended to be resident within the aneurysm after it is deployed. After deployment, the aneurysm may be at least partially filled with vaso-occlusive devices such as helically wound coils.
Owner:STRYKER EURO OPERATIONS HLDG LLC +1

Self-expandable aneurysm filling device, system and method of placement

The self-expandable aneurysm filling device, system and method provide for placement of the stent into an aneurysm to at least partially fill and stabilize the aneurysm. The self-expandable aneurysm filling device has a compressed undeployed configuration and an expanded three-dimensional deployed configuration, and a severable deployment junction releasably connects the self-expandable aneurysm filling device to a pusher wire. The severable deployment junction can be mechanically, electrolytically, or thermally severed to separate the self-expandable aneurysm filling device from the pusher wire.
Owner:PENUMBRA

Stent graft with branch leg

The present invention is directed to a system, apparatus, and method for treating, repairing, and / or replacing an aneurysm, preferably an aortic aneurysm, and most preferably, an abdominal aortic aneurysm. The systems, devices, and methods of the present invention include a first prosthesis or stent gasket, and at least one second prosthesis for bypassing the aneurysm. In preferred embodiments, the second prosthesis includes a branch leg that may be disposed and anchored in an either a cross artery or a downstream artery to facilitate fluid flow. In other preferred embodiments, at least one third prosthesis is provided for establishing a fluid flow channel through a second diseased artery to bypass an aneurysm disposed therein. In accordance with the invention, the first artery may be the abdominal aorta and the second artery may be an iliac artery.
Owner:CARDINAL HEALTH SWITZERLAND 515 GMBH

Tapered endovascular stent graft and method of treating abdominal aortic aneurysms and distal iliac aneurysms

The present invention relates to an improved endovascular stent. The endovascular stent is to be used in treating abdominal aortic aneurysms. The endovascular stent has a tapered section which allows it to accommodate markedly large aortas such as the abdominal aorta and still connect to standard modular aortic stent grafts. Methods of utilizing the stent to treat abdominal aortic aneurysms and distal iliac aneurysms are also provided.
Owner:COOK MEDICAL TECH LLC

Endovascular aneurysm treatment device and method

An self-expanding frame is mounted on the distal end of a shaft. The frame is sized and configured so that it can be inserted into the cavity of an aneurysm. Suction is applied to the interior of the aneurysm through the shaft or through another catheter, and the wall of the aneurysm is collapsed onto the exterior surface of the frame. The frame is then collapsed upon further suction being applied to the interior of the aneurysm, which collapses the aneurysm wall with it. The frame folds down on itself, carrying with it the aneurysm wall. The frame is detachable from the shaft and can be left in the collapsed aneurysm.
Owner:UNIV OF LOUISVILLE RES FOUND INC

Implantable intraluminal device and method of using same in treating aneurysms

An intraluminal device implantable in a blood vessel having an aneurysm therein in the vicinity of a perforating vessel and / or of a bifurcation leading to a branch vessel. The intraluminal device includes a mesh-like tube of bio-compatible material having an expanded condition in which the tube diameter is slightly larger than the diameter of the blood vessel in which it is to be implanted, and the tube length is sufficient to straddle the aneurysm and to be anchored to the blood vessel on the opposite sides of the aneurysm. The mesh-like tube also has a contracted condition wherein it is sufficiently flexible so as to be easily manipulatable through the blood vessel to straddle the aneurysm. In its expanded condition, the mesh-like tube has a porosity index of 55%-80% such as to reduce the flow of blood through its wall to the aneurysm sufficiently to decrease the possibility of rupture of the aneurysm but not to unduly reduce the blood flow to a perforating or branch vessel to the degree likely to cause significant damage to tissues supplied with blood by such perforating or branch vessel.
Owner:STRYKER CORP

Biluminal endovascular graft system

InactiveUS7112217B1Great cross-sectional areaStentsBlood vesselsRepair aneurysmIliac Aneurysm
An endovascular graft system used to repair aneurysms in arteries which bifurcate such as the aorta which bifurcates at the aortoiliac junction. The graft system includes two legs, each defining a lumen. Each leg comprises an aortic stent, a graft component and an iliac stent. The graft component is affixed at one end to the aortic stent and at the other end to the iliac stent. Each leg of the graft system is preferably a mirror image of the other with the exception of the aortic stents. The graft component of each leg includes a means for allowing in situ adjustment of the length of the leg to accommodate the different sizes required for different patients.
Owner:CARDINAL HEALTH SWITZERLAND 515 GMBH

Vascular remodeling device

ActiveUS20100023105A1StentsDilatorsMedicineEfferent
A generally spherical vascular remodeling device is permanently positionable at a junction of afferent and efferent vessels of a bifurcation having an aneurysm. After positioning the device at the junction to substantially conform the device to the shape of the junction, the device acts as a scaffolding to inhibit herniation of objects out of the aneurysm and the device permits perfusion to the efferent vessels. Positioning the device may include deployment and mechanical or electrolytic release from a catheter. Embolic material may be inserted in the aneurysm before or after positioning the device. The device may have a first end, a second end substantially opposite to the first end, and a plurality of filaments extending between and coupled at the first end and the second end. Such devices may be football shaped, pumpkin shaped, or twisted. The device may include a plurality of loops forming a generally spherical shape.
Owner:TYCO HEALTHCARE GRP LP

Detachable balloon embolization device and method

An endovascular aneurysm occlusion device comprising a detachable balloon assembly. The balloon assembly is comprised of an outer balloon and an inner balloon. The outer balloon is formed from a porous material. The occlusion device is expanded within an aneurysm and adhesive material is injected into and perfused through the outer balloon. The adhesive material forms a bond between the aneurysm, the outer balloon, and the inner balloon. The inner balloon is then deflated, which acts to reduce the size of the aneurysm.
Owner:CODMAN & SHURTLEFF INC

Aneurysm neck cover for sealing an aneurysm

An aneurysm neck cover is disclosed for use in occluding the flow of blood within an aneurysm. The aneurysm neck cover includes a first and second expandable sealing member having a circular joining member and reinforcing spokes which give the sealing members a slightly cupped configuration. The expandable sealing members are connected with a support element. When the aneurysm neck cover is deployed within the aneurysm, the first sealing member expands within the aneurysm while the second sealing member expands within an adjacent blood vessel thereby forming a seal around the mouth of the aneurysm and preventing the flow of blood within the aneurysm.
Owner:CODMAN & SHURTLEFF INC

Supra-renal prosthesis and renal artery bypass

The present invention is a system, apparatus, and method for treating, repairing, and / or replacing an aneurysm, preferably an aortic aneurysm, the most preferably, an abdominal aortic aneurysm. The systems, devices, and methods of the present invention include a first prosthesis or stent gasket, and at least one second prosthesis for bypassing the aneurysm, and at least one third prosthesis for establishing a fluid flow channel from the abdominal aorta into another artery, such as a renal artery.
Owner:CARDINAL HEALTH SWITZERLAND 515 GMBH

Supra-renal anchoring prosthesis

ActiveUS7326237B2StentsBlood vesselsProsthesisRepair aneurysm
A system, apparatus, and method for treating, repairing, an aneurysm, preferably an aortic aneurysm, and most preferably, an abdominal aortic aneurysm as described herein. The systems, devices, and methods described herein include a first prosthesis or stent gasket, and at least one second prosthesis for bypassing the aneurysm. The first prosthesis is configured and adapted to accommodate a section of artery upstream of the aneurysm, wherein the section is unsuitable for anchoring a typical first prosthesis.
Owner:CARDINAL HEALTH SWITZERLAND 515 GMBH

Aneurysm embolic device with an occlusive member

An aneurysm embolic device is disclosed for use in occluding the flow of blood within an aneurysm. The aneurysm embolic device includes an expandable sealing member having a circular joining member and reinforcing spokes which give the sealing member a slightly cupped configuration. The embolic device also includes an occlusive member carried by the expandable sealing member. When the aneurysm embolic device is deployed within the aneurysm, the sealing member expands and the occlusive member fills the aneurysm preventing the flow of blood within the aneurysm.
Owner:CODMAN & SHURTLEFF INC

Intravascular methods and apparatus for isolation and selective cooling of the cerebral vasculature during surgical procedures

Patients having diminished circulation in the cerebral vasculature as a result of stroke or from other causes such as cardiac arrest, shock or head trauma, or aneurysm surgery or aortic surgery, are treated by flowing an oxygenated medium through an arterial access site into the cerebral vasculature and collecting the medium through an access site in the venous site of the cerebral vasculature. Usually, the cold oxygenated medium will comprise autologous blood, and the blood will be recirculated for a time sufficient to permit treatment of the underlying cause of diminished circulation. In addition to oxygenation, the recirculating blood will also be cooled to hypothermically treat and preserve brain tissue. Isolation and cooling of cerebral vasculature in patients undergoing aortic and other procedures is achieved by internally occluding at least the right common carotid artery above the aortic arch. Blood or other oxygenated medium is perfused through the occluded common carotid artery(ies) and into the arterial cerebral vasculature. Usually, oxygen depleted blood or other medium leaving the cerebral vasculature is collected, oxygenated, and cooled in an extracorporeal circuit so that it may be returned to the patient. Occlusion of the carotid artery(ies) is preferably accomplished using expansible occluders, such as balloon-tipped cannula, catheters, or similar access devices. Access to the occlusion site(s) may be open surgical, percutaneous, or intravascular.
Owner:BARBUT DENISE +3

Vascular remodeling device

Described herein are vascular remodeling devices that include a proximal section, an intermediate section, and a distal section. During deployment, the proximal section can expand from a compressed delivery state to an expanded state and anchors the device in an afferent vessel of a bifurcation. The distal section expands from the compressed delivery state to an expanded state that may be substantially planar, approximately semi-spherical, umbrella shaped, or reverse umbrella shaped. The distal section is positioned in a bifurcation junction across the neck of an aneurysm or within an aneurysm. The intermediate section allows perfusion to efferent vessels. Before or after the device is in position, embolic material may be used to treat the aneurysm. The distal section can act as a scaffolding to prevent herniation of the embolic material. The device can be used for clot retrieval with integral distal embolic protection.
Owner:TYCO HEALTHCARE GRP LP

Systems and methods for deploying a biosensor with a stent graft

A stent graft includes a tubular prosthetic graft, a support structure expandable between contracted and enlarged conditions, and a biosensor attached thereto. The biosensor may be directly attached to an outer surface of the graft, to struts defining the support structure, or by one or more filaments configured to dispose the biosensor beyond an outer surface of the stent graft. When the biosensor is attached by one or more filaments, the stent graft is mounted in a contracted profile on a delivery apparatus with the biosensor disposed adjacent to the stent graft thereon. The stent graft is introduced into a blood vessel in the contracted profile, and advanced endolumenally until it is positioned across an aneurysm. The stent graft is expanded towards an enlarged profile such that ends of the stent graft engage healthy regions of the vessel adjacent to the aneurysm, thereby isolating the aneurysm from the rest of the vessel with the biosensor disposed within the aneurysmal sac, the biosensor allowing remote monitoring of pressure or other conditions to detect an endoleak or excessive pressure therein.
Owner:REMON MEDICAL TECH
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