FDA Clears Nexstim's Navigated Brain Stimulation For Non-invasive Cortical Mapping Prior To Neurosurgery
Main Category: Neurology / NeuroscienceAlso Included In: Regulatory Affairs / Drug Approvals
Article Date: 13 Dec 2009 - 0:00 PDT
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Nexstim Oy, a medical device company, announced that the U.S. Food and Drug Administration (FDA) has cleared the Navigated Brian Stimulation System for use in the assessment of the primary motor cortex for pre-procedural planning.
Using transcranial magnetic stimulation (TMS) guided by standard MR-image data, Nexstim has developed Navigated Brian Stimulation (NBS), the first non-invasive direct technique for functional mapping of the motor cortex. In its FDA submission, Nexstim included data comparing the accuracy of NBS pre-operative mapping with the results of "gold standard" direct cortical stimulation during actual brain tumor surgery.
Neurosurgeons have long awaited a reliable, non-invasive, tool for pre-operative planning as an alternative to direct cortical stimulation, an invasive technique which is performed after craniotomy at the beginning of surgery. Cortical mapping with NBS is a major advance that may help in tailoring neurosurgical treatment and planning to the needs of the individual patient - potentially saving valuable time in the OR and helping ensure the best possible outcome for the patient.
Lothar Koob, Chairman of the Board of Nexstim commented, "This first FDA clearance for Nexstim marks an important milestone in the development of the company, and based on very encouraging feedback from clinicians we see many additional potential applications for our proprietary navigated brain stimulation technologies."
Source
Nexstim
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MLA
13 Feb. 2012. <http://www.medicalnewstoday.com/releases/173792.php>
APA
http://www.medicalnewstoday.com/releases/173792.php.
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