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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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