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Preclinical Testing of eSVS Mesh*
The eSVS Mesh has been studied in a variety of preclinical models to confirm that the device performs as expected. These animal trials showed a statistically significant inhibition of the formation of intimal hyperplasia when the eSVS Mesh was used with an SVG in CABG procedures.** Preclinical trials of the eSVS Mesh technology have been presented in peer-reviewed journals including The Journal of Thoracic and Cardiovascular Surgery in February 2008 and the Journal of Vascular Surgery in June 2009.
SHEEP MODEL HISTOLOGY AT 180 DAYS
Untreated SVGMid-grafts cross-sections and histological staining showing intimal proliferation and thrombus formation with luminal reduction.
SVG with the eSVS Mesh
Mid-graft sections and histological stain showing normal intimal and fully functioning endothelial layer with no luminal loss.
Caution: Investigational Device Limited by Federal (or United States) law to investigational use
This device is commercially available for use in select international markets
** Human clinical studies may not be consistent with animal trial results.