FDA 510(k) Applications Submitted by ROBERT M WOLFARTH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K981053	03/23/1998	KODAK DIGITAL SCIENCES (KDS) IMAGE VIEW	EASTMAN KODAK COMPANY
K040803	03/29/2004	MS-30 FEMORAL STEM STANDARD AND LATERAL	ZIMMER, INC.
K050699	03/18/2005	MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004	AMEDICA CORP.
K030923	03/24/2003	EPSILON DURASUL CONSTRAINED ACETABULAR LINER	CENTERPULSE ORTHOPEDICS, INC.
K031183	04/15/2003	TIBIAL SPACER FOR THE NATURAL-KNEE II CEMENTED MODULAR TIBIAL BASEPLATE	CENTERPULSE ORTHOPEDICS, INC.
K091278	05/01/2009	VALEO SPACER SYSTEM	AMEDICA CORP.
K051525	06/08/2005	ARX SPINAL SYSTEM	AMEDICA CORP.
K992056	06/18/1999	ANNULOFLEX ANNULOPLASTY SYSTEM, MODEL AF800	SULZER CARBOMEDICS, INC.
K121892	06/29/2012	PHANTOM PLUS CERAMIC CAGE SYSTEM	AMEDICA CORP.
K032348	07/30/2003	CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUP	CENTERPULSE ORTHOPEDICS, INC.
K032380	08/01/2003	WAGNER CONE PROSTHESIS	CENTERPULSE ORTHOPEDICS, INC.
K022892	08/30/2002	ASCENSION SILLICONE MCP	ASCENSION ORTHOPEDICS, INC.