Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K961970 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker Bur Guard REF 2296-301, Stryker Instruments, Kalamazoo, MI (USA) The Impaction Bur Guard is... | 2 | 09/13/2010 | Stryker Instruments Div. of Stryker Corporation |
| Stryker Impaction Bur Guard REF 2296-301, 2296-300, 0260-901-300, & 5400-300; Stryker Instruments, K... | 2 | 03/30/2009 | Stryker Instruments Div. of Stryker Corporation |
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