A case of stenting for acute cerebral venous sinus thrombosis in the superior sagittal sinus

Trevo ™ XP ProVue Retrievers INDICATIONS FOR USE The Trevo Retriever is intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke within 8 hours of symptom onset.Patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment.AXS Catalyst ™ Distal Access Catheter INTENDED USE/INDICATIONS FOR USE The AXS Catalyst Distal Access Catheter is indicated for use in facilitating the insertion and guidance of appropriately sized interventional devices into a selected blood vessel in the peripheral and neurovascular systems.It is also indicated for the removal/ aspiration of soft emboli and thrombi from vessels in the peripheral and neurovasculature.FlowGate 2™ Balloon Guide Catheter INDICATIONS FOR USE FlowGate 2™ Balloon Guide Catheters are indicated for use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neuro vascular systems.The balloon provides temporary vascular occlusion during these and other angiographic procedures.The Balloon Guide Catheter is also indicated for use as a conduit for Retrieval devices. THIS DOCUMENT IS INTENDED SOLELY FOR THE USE OF HEALTHCARE PROFESSIONALS.A physician must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when treating a particular patient.Stryker does not dispense medical advice and recommends that physicians be trained in the use of any particular product before using it in a procedure.The information presented is intended to demonstrate the breadth of Stryker product offerings.A physician must always refer to the package insert, product label and/or instructions for use before using any Stryker product.Products may not be available in all markets because product availability is subject to the regulatory and/or medical practices in individual markets.Please contact your Stryker representative if you have questions about the availability of Stryker products in your area.The Stryker products listed above are CE marked according to the Medical Device Directive 93/42/EEC.