FDA 510(k) Applications Submitted by ROAIDA RIZKALLAH

FDA 510(k) Number Submission Date Device Name Applicant
K100122 01/15/2010 MODIFICATION TO CAPSURE PS SYSTEM SPINE WAVE, INC.
K090315 02/09/2009 STAXX XD SYSTEM SPINE WAVE, INC.
K120646 03/02/2012 CAPSURE(R) PS SYSTEM SPINE WAVE, INC.
K131071 04/17/2013 STAXX IBL SYSTEM SPINE WAVE, INC.
K081228 04/30/2008 CAPSURE PS (R) SPINE SYSTEM SPINE WAVE, INC.
K101288 05/07/2010 STAXX XD SYSTEM SPINE WAVE, INC.
K111418 05/20/2011 STAXX(R) XD SYSTEM SPINE WAVE, INC.
K011987 06/26/2001 MODIFIED M-IV MAMMOGRAPHY SYSTEM LORAD, A HOLOGIC CO.
K121889 06/28/2012 STAXX XD SYSTEM SPINE WAVE, INC.
K111913 07/06/2011 CAPSURE(R) PS SYSTEM SPINE WAVE, INC.
K132719 08/30/2013 STAXX IBL SYSTEM SPINE WAVE, INC.
K013290 10/02/2001 MODIFIED 650 MAMMOGRAPHY SYSTEM LORAD, A HOLOGIC CO.
K123461 11/09/2012 STAXX(R) IB SYSTEM SPINE WAVE, INC.
K083353 11/13/2008 CAPSURE(R) PS SYSTEM SPINE WAVE, INC.
K083743 12/16/2008 CAPSURE PS SYSTEM SPINE WAVE, INC.


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