FDA 510(k) Applications Submitted by TONI KINGSLEY

FDA 510(k) Number Submission Date Device Name Applicant
K060556 03/02/2006 BRIGIT SURGICAL DEVICE ZIMMER INC.
K050723 03/21/2005 MG II TOTAL KNEE SYSTEM STEMMED TIBIAL BASEPLATE COMPONENTS ZIMMER, INC.
K081860 07/01/2008 ZIMMER SEGMENTAL SYSTEM VARIABLE STIFFNESS STEM EXTENSIONS AND INTERCALARY SEGMENTS ZIMMER, INC.


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