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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K894124
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FDA Recall
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Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker France Both the ... 2 12/11/2013 Stryker Howmedica Osteonics Corp.
Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw Ref 2030-6525-1 The 6.5mm Cancellous Bo... 2 11/19/2012 Stryker Howmedica Osteonics Corp.
Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw Ref 2030-6535-1 The 6.5mm Cancellous Bo... 2 11/19/2012 Stryker Howmedica Osteonics Corp.
6.5 Cancellous Bone Screw 25 mm; Responsible Firm on Label: Manufacturer, Howmedica Osteonics Corp.,... 2 09/22/2008 Stryker Howmedica Osteonics Corp.
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