FDA 510(k) Applications Submitted by JASON LIPMAN

FDA 510(k) Number Submission Date Device Name Applicant
K110604 03/03/2011 VBB SYSTEM SYNTHES
K090605 03/06/2009 CLAMPFIX SYNTHES (USA)
K100952 04/06/2010 MODIFICATION TO SYNTHES MATRIX SYSTEM SYNTHES SPINE
K082572 09/05/2008 USS ILIOSACRAL, USS POLYAXIAL SYNTHES SPINE
K082914 09/30/2008 CLAMPFIX SYNTHES SPINE


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