FDA 510(k) Applications Submitted by WHITESIDE BIOMECHANICS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K033313 10/15/2003 QUATRO M FEMORAL COMPONENT WHITESIDE BIOMECHANICS, INC.
K991678 05/17/1999 WHITESIDE BIOMECHANICS SPINAL SYSTEM WHITESIDE BIOMECHANICS, INC.
K012800 08/21/2001 SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM WHITESIDE BIOMECHANICS, INC.
K993903 11/16/1999 WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013 WHITESIDE BIOMECHANICS, INC.
K003618 11/22/2000 WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014 WHITESIDE BIOMECHANICS, INC.
K981238 04/03/1998 BIPOLAR FEMORAL HEAD WHITESIDE BIOMECHANICS, INC.
K961625 04/26/1996 QUATROLOC FEMORAL COMPONENT & HEAD WHITESIDE BIOMECHANICS, INC.
K971718 05/09/1997 MICRO-SEAL ACETABULAR SYSTEM WHITESIDE BIOMECHANICS, INC.
K971721 05/09/1997 WHITESIDE BIOMECHANICS, INC. ZIRCONIA CERAMIC FEMORAL HEAD WHITESIDE BIOMECHANICS, INC.
K973261 08/29/1997 WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD WHITESIDE BIOMECHANICS, INC.
K964150 10/16/1996 WHITESIDE BIOMECHANICS ZIRCONIA CERAMIC FEMORAL HEAD WHITESIDE BIOMECHANICS, INC.
K961157 03/22/1996 WHITESIDE BIOMECHANICS CANCELLOUS BONE SCREW WHITESIDE BIOMECHANICS, INC.
K964616 10/24/1996 QUATROLOC PLASMA SPRAYED FEMORAL COMPONENT WHITESIDE BIOMECHANICS, INC.


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