Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K070095 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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. |
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