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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 17 of 17 Results
510(K) Number: K082924
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DYNASTY(R) BIOFOAM(R) SHELL, SIZE: 64mm GROUP H, REF DSBFGH64, Rx ONLY, STERILE R, Wright Medical T... 2 02/14/2012 Wright Medical Technology Inc
DYNASTY(R) BIOFOAM(R) SHELL, SIZE: 66mm GROUP H, REF DSBFGH66, Rx ONLY, STERILE R, Wright Medical T... 2 02/14/2012 Wright Medical Technology Inc
DYNASTY(R) BIOFOAM(R) SHELL, SIZE: 68mm GROUP H, REF DSBFGH68, Rx ONLY, STERILE R, Wright Medical T... 2 02/14/2012 Wright Medical Technology Inc
DYNASTY(R) BIOFOAM(R) SHELL, SIZE: 70mm GROUP J, REF DSBFGJ70, Rx ONLY, STERILE R, Wright Medical T... 2 02/14/2012 Wright Medical Technology Inc
DYNASTY(R) BIOFOAM(R) SHELL, SIZE: 72mm GROUP J, REF DSBFGJ72, Rx ONLY, STERILE R, Wright Medical T... 2 02/14/2012 Wright Medical Technology Inc
DYNASTY(R) BIOFOAM(R) SHELL, SIZE: 74mm GROUP J, REF DSBFGJ74, Rx ONLY, STERILE R, Wright Medical T... 2 02/14/2012 Wright Medical Technology Inc
DYNASTY® A-CLASS® POLY LINER, REF DLXP-LD36, 1 EACH, Rx ONLY, STERILE EO, GROUP D, I.D. 36 mm, LIP 1... 3 08/12/2010 Wright Medical Technology Inc
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