The flexible strength of the VBX Stent Graft helps you address the treatment challenges in complex iliac occlusive disease. 

The cases presented here feature a range of conditions and procedures that demonstrate the proven performance of the VBX Stent Graft. Watch for new cases.
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Treating severe aortoiliac occlusive disease (AIOD) at the aortic bifurcation

In this bilateral common iliac artery case submitted by Jean Panneton, M.D., see the VBX Stent Graft treat complex AIOD with long-term durability.
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Restoring flow in a patient with severe claudication and focal iliac calcification

A case from Chris Metzger, M.D., presents a severe intermittent claudication (Rutherford 3) TASC II B lesion in the right common iliac artery (CIA) and focal iliac calcification to improve flow and patient symptoms.
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Restoring flow at the aortic bifurcation

In this bilateral common iliac case submitted by Masahiko Fujihara, M.D., see VBX Stent Grafts deployed in a kissing stent technique to restore flow at the aortic bifurcation.
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Reconstructing the aortic bifurcation

In a TASC II Type C lesion, “kissing” placement of the VBX Stent Graft successfully reconstructs the aortic bifurcation.
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Treating a severely calcified lesion

In this severely calcified lesion case, see the “up and over” deployment and post-procedure results with the VBX Stent Graft.
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Achieving conformability and durable results in tortuous anatomy

In this bilateral proximal common iliac case, see VBX Stent Graft conform to tortuous anatomy to produce widely patent arteries.
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Procedural outcomes based on usage of legacy GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis. (BXA catalogue numbers).

IFU Consult instructions

Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the market where this product is available. RXOnly 

GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis

INDICATIONS FOR USE IN EUROPE: The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of:

  • de novo or restenotic lesions in the iliac arteries, including lesions at the aortic bifurcation;
  • de novo or restenotic lesions in the visceral arteries;
  • isolated visceral, iliac, and subclavian artery aneurysms; or
  • traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries). 

The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for use as a bridging stent in branched and fenestrated endovascular aortic aneurysm repair with the following:

  • Approved for use branched aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and polypropylene suture with branch diameters of 6/8 mm and lengths of 18/21 mm.
  • Approved for use fenestrated aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and fenestrations with polypropylene suture ranging in diameter from 6–8 mm. 

CONTRAINDICATIONS: Do not use the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II.

 

GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (Reduced Profile):

INDICATIONS FOR USE IN EUROPE: The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of: 

  • de novo or restenotic lesions in the iliac arteries, including lesions at the aortic bifurcation;  
  • de novo or restenotic lesions in the visceral arteries;  
  • isolated visceral, iliac, and subclavian artery aneurysms; or
  • traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries). 

CONTRAINDICATIONS: Do not use the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II. 

Product may not be available in all countries. Please check with your Gore representative for availability.
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