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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K955599
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Product Description
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FDA Recall
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Femoral Sponge 10 inches REF 206-715, Rx Sterile, Stryker Instruments Kalamazoo, MI. The femoral ... 2 03/15/2010 Stryker Instruments Div. of Stryker Corporation
Bio-Prep Bone Preparation Kit with Merocel sponge for use in total hip arthroplasty. REF 206-730, R... 2 03/15/2010 Stryker Instruments Div. of Stryker Corporation
ACM Bio-Prep with Merocel pkg/6, Rx, Sterile, REF 0306-708-000S4, Stryker Instruments, Kalamazoo, MI... 2 03/15/2010 Stryker Instruments Div. of Stryker Corporation
ACM with Femoral Brush and Femoral Sponge, Rx, Sterile, REF 306-705-000S8, Stryker Instruments, Kal... 2 03/15/2010 Stryker Instruments Div. of Stryker Corporation
Advanced Cement Mixing Bio-Prep Cement Application Kit, Rx, Sterile, REF 306-563S10, Stryker Instru... 2 03/15/2010 Stryker Instruments Div. of Stryker Corporation
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