FDA 510(k) Applications Submitted by JUDITH ROSEN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120990	04/02/2012	NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIAL CONES PROVISIONALS TO NEXGEN LCCK TRABECULAR METAL (TM) COUPLED TIBIAL	ZIMMER TRABECULAR METAL TECHNOLOGY
K123602	11/21/2012	TM ARDIS INTERBODY SYSTEM INSERTER	ZIMMER TRABECULAR METAL TECHNOLOGY
K103517	11/30/2010	TRABECULAR METAL FEMORAL CONE AUGMENTS	ZIMMER TRABECULAR METAL TECHNOLOGY, INC.
K113561	12/01/2011	TM ARDIS INTERBODY SYSTEM TM ARDIS INTERBODY SYSTEM INSTRUMENATION	ZIMMER TRABECULAR METAL TECHNOLOGY
K133784	12/12/2013	VISTA-S DEVICE, ASSOCIATED INSTRUMENTATION	ZIMMER TRABECULAR METAL TECHNOLOGY