The Supera™ Peripheral Stent is a unique class of SFA Technology. Engineered with an innovative interwoven wire technology, this nitinol stent offers physicians unmatched clinical outcomes1-12 across varied lesion complexities and lengths.1, 13-15
The Supera™ Stent is known for the excellence of its clinical outcomes after percutaneous transluminal angioplasty (PTA) procedures with stent placement, since this peripheral stent has been studied in more than 2,000 patients and 17 studies worldwide.1,15-30
When nominally deployed*
When nominally deployed*
*Nominal deployment is defined as the stent length upon deployment being within +/- 10% of the labeled stent length. This data is from a non-powered post-hoc analysis.
Supera™ Stent demonstrated excellent 1 yr patency and 3 yr freedom from TLR in the SUPERB trial.1
Demonstrated unmatched clinical outcomes in simple lesions1-12
Exhibits consistent 1-year primary patency results regardless of lesion length13-20,31
Reveals strong clinical outcomes in severely calcified lesions at year 3 years1
Study reported 93.8% with Trans-Atlantic Inter-Society Consensus Document (TASC) A & B lesions and/or Rutherford class 2 or 3 lesions
*Patency rates have been evaluated in studies in lesion lengths ranging from 5.3 cm to 28.0 cm.
Unlike any other stent design platform, the Supera™ Stent is uniquely designed to keep vessels open with its distinct platform, created by interwoven individual, flexible nitinol wires.
4x greater strength for compression resistance—so it can maintain a round, open lumen, which can be especially beneficial in calcified lesions
With 1:1 stent to vessel sizing, low chronic outward force results in minimal vessel injury34
Unparalleled flexibility,33 which mimics the natural structure and movement of the anatomy35-37
Zero stent fractures reported at 1 year in over 2,000 patients across 17 studies1,15-30
MAT-2106530 v2.0
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MAT-2305078 v1.0