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Clinical Trial

Case-Specific Health Care Professional Clinical Survey for Concerto Versa™ Detachable Coils

NCT: NCT07639853 · ENROLLING_BY_INVITATION

NCT IDNCT07639853
StatusENROLLING_BY_INVITATION
Start Date2026-07-24
SponsorMedtronic Endovascular (INDUSTRY)
First posted
Last updated

Brief Summary

The purpose of the Case-Specific Health Care Professional (HCP) Clinical Survey for Concerto Versa™ Detachable Coils, also known as the Concerto Versa HCP Clinical Assessment, is to collect early clinical data from HCPs to assess clinical safety and performance of the Concerto Versa™ Detachable Coils, when used in accordance with approved device labeling per the Instructions for Use (IFU). Data collected will generate clinical evidence to quantitatively assess clinical safety and device performance for the purpose of obtaining European Union Medical Device Regulation (EU MDR) approval.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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