18 Years to 90 Years
Male or Female
A prospective, single-arm, non-blinded study, intending to collect and evaluate data in up to forty (40) human subjects with acute thrombosis, treated with the CAPERE™ Thrombectomy System. The CAPERE™ Thrombectomy System is designed to achieve clot retrieval with one (1) treatment session. The CAPERE™ system is cleared for market in the United States and this study is intended to capture real-world clinical data as part of CAPERE™ post-market clinical follow up.
For further information about this study or to express your interest in this study, please fill out and submit this form.
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