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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 13 of 13 Results
510(K) Number: K070095
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FDA Recall
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Offset Adaptor Trial - 8MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteonics Corp: ... 2 07/23/2009 Stryker Howmedica Osteonics Corp.
Triathlon-Press-Fit Stem These devices are modular components of a total knee system. These modul... 2 01/26/2009 Stryker Howmedica Osteonics Corp.
Triathlon X3 Total Stabilizer + Tibial Insert For use with Triathlon Universal Baseplates, knee p... 2 09/25/2007 Stryker Howmedica Osteonics Corp.