Ovation 1C31179G01 Module

Original New PLC Module 1C31179G01 In Stock

Description

Accurate fluoroscopic imaging is required during any endovascular procedure and for proper device deployment. Implantation of this device should occur in an operating room, endovascular suite, catheterization laboratory, or similar sterile environment, with appropriately trained personnel, and suitable equipment and imaging capabilities. Do not use this device if the patient is unable to be evaluated using the necessary preoperative and postoperative imaging. Always have a qualified surgery team available during implantation or re-intervention procedures in the event that conversion to open surgical repair is necessary. The TriVascular Ovation iX Abdominal Stent Graft System should only be used by physicians and teams experienced in endovascular techniques and who have been trained in its use. The long-term performance of this implant has not been established. All patients treated with this device must undergo periodic imaging to evaluate stent graft integrity and position, aneurysm size, and potential endoleaks and/or, occlusion of vessels in the treatment area. Significant aneurysm enlargement, a persistent endoleak, the appearance of a new endoleak, device migration, reduced blood flow through the graft, and/or decrease in renal function due to renal artery occlusion should prompt further investigation into the need for further patient treatment, including additional intervention or surgical conversion. Additional patient imaging follow up should be considered for patients with devices that have effectiveness issues. All patients should be carefully counseled on the need for long-term follow up. The device is not recommended in patients unable or unwilling to comply with the information in Follow-up Imaging Recommendations.

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