Observational Study Clinical Trial
Official title:
CAPERE Thrombectomy System Post-Market Clinical Follow Up Study
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.
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. Subjects will be evaluated based on VEINES QoL survey pre- and post-treatment (30-days). ;
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