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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