Rx Only.

INDICATIONS:

The NEXUS^® Aortic Arch Stent Graft System is indicated for the endovascular treatment of chronic dissections involving the aortic arch in patients who are at high risk for open surgical repair and who have appropriate anatomy including:

• Adequate iliac or femoral artery access vessel morphology that is compatible with vascular access techniques, devices, or accessories.

• Proximal/ascending native landing zone aortic anatomy including: 30 mm to 39 mm diameter; ≥ 30 mm length; Landing zone cannot be aneurysmal, dissected, heavily thrombosed and tortuous.

• Proximal/ascending previously implanted surgical graft landing zone including: 26 mm to 39 mm diameter; ≥ 30 mm length.

• Brachiocephalic trunk native landing zone anatomy including: 12.5 mm to 19.5 mm diameter; ≥ 20 mm length, Landing zone cannot be aneurysmal, dissected, heavily thrombosed and tortuous.

• Distal/descending native landing zone aortic anatomy including: 28 mm to 42 mm diameter; ≥ 30 mm length.

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CONTRAINDICATIONS:

The NEXUS^® Aortic Arch Stent Graft System is contraindicated for use in:

• Patient with known sensitivities or allergies to the device materials;

• Patient who has a condition that threatens to infect the graft.

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WARNINGS AND PRECAUTIONS:

Refer to the complete “Directions for Use” for more information on Warnings, Precautions, Adverse Events, and Operator’s Instructions.

 

Review full Indications, Safety, and Warnings.

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MKE-0002718 Rev. 13 MAY 2026