FDA 510(k) Applications Submitted by LUIS NESPRIDO

FDA 510(k) Number Submission Date Device Name Applicant
K000009 01/03/2000 SPIRAL RADIUS RODDING SYSTEM UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K071376 05/17/2007 MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM VERTEBRON, INC.
K081567 06/04/2008 VERTEBRON SSP CERVICAL PLATING SYSTEM VERTEBRON, INC.
K081597 06/06/2008 MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM VERTEBRON, INC.
K051716 06/27/2005 VERTEBRON PSS PEDICLE SCREW SYSTEM VERTEBRON, INC.
K051815 07/05/2005 MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM VERTEBRON, INC.
K062110 07/24/2006 VERTEBRON SCP CERVICAL PLATE SYSTEM VERTEBRON, INC.
K992784 08/19/1999 NEXT GENERATION RODDING SYSTEM UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC
K043152 11/15/2004 VERTEBRON PSS PEDICLE SCREW SYSTEM VERTEBRON, INC.
K043181 11/17/2004 MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM VERTEBRON, INC.
K073502 12/13/2007 VERTEBRON VBR SYSTEM VERTEBRON, INC.


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