Endologix

Embrace the evidence. Driven by data. Pioneering for patients.

Join us at VEITH 2022
Booth #311
3rd Floor Promenade

9 rapid-fire presentations from world-renowned vascular specialists

Visit Program

Hear about the latest LEOPARD trial – the first prospective, multi-center, randomized controlled trial (RCT) comparing the outcomes of endovascular aneurysm repair (EVAR) using commercially available devices in a real-world population.

Thursday, November 17, 7:56AM-8:01AM
Presented by: Christopher J. Kwolek, MD, MBA

Experience the first-ever EVAR procedural training with virtual reality at VEITHSymposium 2022.

Booth #311
3rd Floor Promenade

VR allows procedural steps to be safely practiced in preparation for real-world scenarios.

VR has been shown to improve surgical performance compared to traditional training.¹

Multiple users can connect globally in real-time, for remote collaboration and learning.

ALTO Abdominal Stent Graft System

An EVAR as unique as your patients

No two patients are alike—the ALTO^® abdominal stent graft system provides a custom seal that conforms to the needs of specialized anatomies.

Learn More

These are a portrayal of typical EVAR patients and not real patients.

Blumstein G. How Virtual Reality Can Help Train Surgeons. Harvard Business Review https://hbr.org/2019/10/research-how-virtual-reality-can-help-train-surgeons

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 > 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 < 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 ≤ 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.

Endologix is a registered trademark of Endologix LLC in the United States, Europe and Japan and ALTO is a registered trademark of Endologix LLC and its subsidiaries. All other trademarks are the property of their respective owners.

Join us at VEITH 2022 Booth #311 3rd Floor Promenade

9

rapid-fire presentations from world-renowned vascular specialists