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Aneurysm Neck Articles & Analysis

6 news found

Cerus Endovascular Announces IDE Approval from the U.S. FDA to Conduct Clinical Study of the Contour Neurovascular System

Cerus Endovascular Announces IDE Approval from the U.S. FDA to Conduct Clinical Study of the Contour Neurovascular System

The study, is designed to develop a robust data set to support the safety and efficacy of the Contour Neurovascular System™ for the endovascular embolization of wide-necked, bifurcated, saccular intracranial aneurysms. Study results will be submitted in a Premarket Approval (PMA) application to the FDA. ...

ByCerus Endovascular Inc.


Cerus Endovascular Receives FDA Breakthrough Device Designation for its Contour Neurovascular System

Cerus Endovascular Receives FDA Breakthrough Device Designation for its Contour Neurovascular System

Indicated for the treatment of intracranial aneurysms, the Contour Neurovascular System™, composed of fine mesh braid, represents a unique intrasaccular advancement in the market, as it targets the neck of the aneurysm, away from the vulnerable dome. Additionally, the System is designed to be self-anchored for stability, re-sheathable for ...

ByCerus Endovascular Inc.


Cerus Endovascular Announces the First Ever Robotic Assist Intracranial Implant of its Contour Intrasaccular Device

Cerus Endovascular Announces the First Ever Robotic Assist Intracranial Implant of its Contour Intrasaccular Device

Nitin Dange and was performed on a Middle Cerebral Aneurysm with a 7mm Contour device. Procedural time, including access and placement of the Contour, took a total of 28 minutes. ...

ByCerus Endovascular Inc.


Cerus Endovascular Receives CE Mark Approval for its  021 Contour Neurovascular System

Cerus Endovascular Receives CE Mark Approval for its 021 Contour Neurovascular System

Cerus Endovascular Ltd., a privately held, commercial stage medical device company, today announced that it has received CE Mark approval for its 021 Contour Neurovascular System, compatible with smaller commercially available 021 microcatheters for the treatment of saccular intracranial aneurysms. The Contour Neurovascular System is a unique, fine mesh braid that is deployed ...

ByCerus Endovascular Inc.


Cerus Endovascular Receives CE Mark Approvals for its Neqstent Coil Assisted Flow Diverter Designed to Treat Intracranial Aneurysms

Cerus Endovascular Receives CE Mark Approvals for its Neqstent Coil Assisted Flow Diverter Designed to Treat Intracranial Aneurysms

Cerus Endovascular Ltd., a privatelyheld, commercial stage medical device company, today announced that it has received CE Mark approval for its Neqstent Coil Assisted Flow Diverter device, designed to treat intracranial aneurysms. Neqstent is designed to treat a range of aneurysm morphologies including wide-necked bifurcation and bifurcation ...

ByCerus Endovascular Inc.


Cerus Endovascular Successfully Completes Series B Financing and Receives U.S. FDA Approval for its First Microcatheter

Cerus Endovascular Successfully Completes Series B Financing and Receives U.S. FDA Approval for its First Microcatheter

Completion of the Series B financing will allow the company to execute on its go-to-market strategy and to complete the planned expansion of its product portfolio, which will include a smaller delivery platform for its recently CE Marked lead product, the Contour Neurovascular System, for the treatment of intracranial aneurysms. The company’s second implant device, the ...

ByCerus Endovascular Inc.

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