FDA 510(k) Applications Submitted by VINEET SARIN

FDA 510(k) Number Submission Date Device Name Applicant
K010101 01/11/2001 GEM POSTERIOR STABILIZED TOTAL KNEE SYSTEM KINAMED, INC.
K030256 01/24/2003 ISO-ELASTIC CERCLAGE SYSTEM KINAMED, INC.
K032950 09/22/2003 GEM INSET PATELLAR COMPONENT KINAMED, INC.
K013982 12/03/2001 KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT KINAMED, INC.
K020764 03/07/2002 NAVIPRO KINAMED, INC.
K050897 04/08/2005 NAVIPRO SHOULDER SOFTWARE MODULE KINAMED, INC.
K072250 08/13/2007 SUPERCABLE GRIP AND PLATE SYSTEM KINAMED, INC.
K033668 11/21/2003 NAVIPRO KNEE SOFTWARE MODULE KINAMED, INC.


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