ALTO Deployment Animation MM 2200 Rev 02

Animation featuring ALTO deployment steps.

ALTO Abdominal Stent Graft System for AAA
Endovascular Aneurysm Repair (EVAR)
https://endologix.com/

INDICATIONS FOR USE: The ALTO® Abdominal Stent Graft System is indicated for treatment of patients with infrarenal abdominal aortic aneurysms having the vascular morphology suitable for endovascular repair with the device, which includes the following:
∙ Adequate iliac/femoral access compatible with vascular access techniques (femoral cutdown or percutaneous), devices, and/or accessories,
∙ A proximal aortic landing zone for the sealing ring 7 mm below the inferior renal artery.
∙ An aortic sealing zone comprised of healthy aorta defined as:
– Lack of significant thrombus greater than 8 mm in thickness; at any point along the aortic circumference at the level of 7mm below the inferior renal artery,
– Lack of significant calcification at the level of 7 mm below the inferior renal artery,
– Conicity less than 10% as measured from the inferior renal artery to the aorta 7 mm below the inferior renal artery,
– An inner wall diameter of no less than 16 mm and no greater than 30 mm at 7 mm below the inferior renal artery, and
– An aortic angle of less than or equal to 60 degrees
∙ A distal iliac landing zone:
– With a length of at least 10 mm, and
– With an inner wall diameter of no less than 8 mm and no greater than 25 mm.

CONTRAINDICATIONS: The system is contraindicated for use in patients who have a condition that threatens to infect the graft and in patients with known sensitivities or allergies to the device materials including polytetrafluoroethylene [PTFE], polyethylene glycol [PEG]-based polymers, contrast agents, fluorinated ethylene propylene [FEP], titanium, nickel, platinum, or iridium.

Refer to Instructions for Use for more information concerning Indications, Contraindications, Specific Anatomic Considerations, Warnings, Precautions, and Adverse Events.

CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.

NOTE: Not all product components are available in every country. Please consult with your Endologix representative to confirm product availability.

©2020 Endologix LLC. All rights reserved. MM2200 Rev 02