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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