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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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