SUPERA is a different class of stent.  This class is defined by unmatched flexibility and strength, which translates to fracture resistance and the ability to truly support anatomy.  Especially in challenging vessels such as the superficial femoral artery, the popliteal artery, and the biliary ducts the physical characteristics of the SUPERA stent provide a unique treatment option for clinicians.

The SUPERA stent is made with six pair of closed end interwoven nitinol wires with a closed cell geometry, and is delivered via a coaxial catheter-based delivery handle.

SUPERA VERITAS delivers a better solution.

Click on the appropriate link for a Quick Reference Guide and complete Instructions for Use for the SUPERA VERITAS system.

Quick Reference Guide			Instructions for Use
	Europe			Europe

The SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent System is indicated for palliative treatment of biliary stricture produced by malignant neoplasms and peripheral vascular use following failed percutaneous transluminal angioplasty (PTA).  CAUTION:  This device is not yet approved by the FDA for distribution in the United States for peripheral vascular disease.