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FDA 510(k) Applications Submitted by VINEET K 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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