FDA 510(k) Applications Submitted by LAETITIA COUSIN

FDA 510(k) Number Submission Date Device Name Applicant
K060010 01/03/2006 NAUTIFLUX SEDAT
K070148 01/16/2007 GRAFT CONTAINMENT DEVICE NUVASIVE, INC.
K070273 01/29/2007 MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM NUVASIVE, INC.
K060225 01/30/2006 NUVASIVE SPHERX SYSTEM NUVASIVE, INC.
K080472 02/21/2008 SEDAT MYSHELL LITE SEDAT
K071329 05/11/2007 NUVASIVE HELIX ACP SYSTEM NUVASIVE, INC.
K081377 05/16/2008 NUVASIVE SURGICAL MESH SYSTEM NUVASIVE, INC.
K071435 05/23/2007 NUVASIVE OCT SYSTEM NUVASIVE, INC.
K051384 05/27/2005 MODIFICATION TO: NUVASIVE NEUROVISION JJB SYSTEM NUVASIVE, INC.
K081611 06/09/2008 NUVASIVE COROENT SYSTEM NUVASIVE, INC.
K061778 06/26/2006 NUVASIVE SPHERX II SYSTEM NUVASIVE, INC.
K061789 06/26/2006 LATERAL PLATE SYSTEM NUVASIVE, INC.
K051718 06/27/2005 NUVASIVE NEUROVISION JJB SYSTEM NUVASIVE, INC.
K071795 07/02/2007 NUVASIVE COROENT SYSTEM NUVASIVE, INC.
K082070 07/22/2008 NUVASIVE LATERAL PLATE SYSTEM NUVASIVE, INC.
K042034 07/29/2004 NUVASIVE MAXCESS LIGHT GUIDE NUVASIVE, INC.
K062317 08/09/2006 MODIFICATION TO NUVASIVE SPHERX II SYSTEM NUVASIVE, INC.
K082332 08/14/2008 NUVASIVE SPHERX SYSTEM NUVASIVE, INC.
K052210 08/15/2005 NUVASIVE COROENT EXTENSURE SYSTEM NUVASIVE, INC.
K072339 08/20/2007 NUVASIVE ANTERIOR LUMBAR PLATE SYSTEM NUVASIVE, INC.
K072343 08/21/2007 NEUROVISION JJB SYSTEM NUVASIVE, INC.
K062590 09/01/2006 NUVASIVE ACP4 SYSTEM NUVASIVE, INC.
K062765 09/29/2006 MODIFICATION TO NUVASIVE NEUROVISION JJB SYSTEM NUVASIVE, INC.
K053215 11/17/2005 SURGICAL MESH SYSTEM NUVASIVE, INC.
K073275 11/21/2007 NUVASIVE HELIX MINI ACP SYSTEM NUVASIVE, INC.
K073278 11/21/2007 SPINOUS PROCESS PLATE SYSTEM NUVASIVE, INC.
K043405 12/10/2004 NUVASIVE COROENT SYSTEM NUVASIVE, INC.
K053581 12/23/2005 NUVASIVE SMARTPLATE GRADIENT PLUS SYSTEM NUVASIVE, INC.


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