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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.
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