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Whiteside Biomechanics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K033313QUATRO M FEMORAL COMPONENTJuly 28, 2004
K012800SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEMMay 3, 2002
K003618WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014May 23, 2001
K993903WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013February 14, 2000
K991678WHITESIDE BIOMECHANICS SPINAL SYSTEMAugust 12, 1999
K981238BIPOLAR FEMORAL HEADAugust 21, 1998
K973261WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEADNovember 24, 1997
K964616QUATROLOC PLASMA SPRAYED FEMORAL COMPONENTAugust 7, 1997
K971721WHITESIDE BIOMECHANICS, INC. ZIRCONIA CERAMIC FEMORAL HEADJuly 30, 1997
K971718MICRO-SEAL ACETABULAR SYSTEMJuly 23, 1997
K964150WHITESIDE BIOMECHANICS ZIRCONIA CERAMIC FEMORAL HEADDecember 27, 1996
K961625QUATROLOC FEMORAL COMPONENT & HEADSeptember 10, 1996
K961157WHITESIDE BIOMECHANICS CANCELLOUS BONE SCREWMay 17, 1996