FDA 510(k) Applications Submitted by SURGIVISION, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K102101 07/27/2010 SURGIVISION MR COMPATIBLE VENTRICULAR CANNULA SURGIVISION, INC.
K091343 05/06/2009 MRI NEURO DRAPE SURGIVISION, INC.
K091439 05/14/2009 HEAD FIXATION ARC AND TABLE BASE SURGIVISION, INC.
K100836 03/24/2010 CLEARPOINT SYSTEM SURGIVISION, INC.


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