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Clinical Trial Summary

The data collected in this study will be used to support International Regulatory submissions. The study objective is to evaluate the continued safety and efficacy of the AXIUM Progressive Coil System.

This Device has been used clinically at approximately 150 Institutions under FDA 510(k) clearance since April 24, 2007. The device received CE authorization on June 30, 2007. Through December 2007, more than 1000 patients have been treated with the AXIUM Coils.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00703794
Study type Observational [Patient Registry]
Source Medtronic Neurovascular Clinical Affairs
Contact
Status Completed
Phase
Start date June 2008
Completion date January 16, 2012

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