Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K070095 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Offset Adaptor Trial - 6MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteonics Corp: 3... | 2 | 07/23/2009 | Stryker Howmedica Osteonics Corp. |
| Offset Adaptor Trial - 4MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteonics Corp: 3... | 2 | 07/23/2009 | Stryker Howmedica Osteonics Corp. |
| Offset Adaptor Trial - 2MM, Triathlon Revision Instruments. Non-Sterile; Howmedica Osteonics Corp: ... | 2 | 07/23/2009 | Stryker Howmedica Osteonics Corp. |
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