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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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