FDA 510(k) Applications Submitted by CIVCO

FDA 510(k) Number Submission Date Device Name Applicant
K092619 08/26/2009 ETRAX NEEDLE SYSTEM, ETRAX VARIABLE ANGLE NEEDLE GUIDANCE SYSTEM, VIRTUTRAX UNIVERSAL TRACKER CIVCO
K071614 06/13/2007 FIDUCIAL MARKERS CIVCO


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