Medical Device Recalls
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1 result found
510(K) Number: K032601 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Stryker Instruments, Interventional Spine RF MultiGen REF 0406-900-000, Rx only,, Stryker Instrument... | 2 | 01/18/2011 | Stryker Instruments Div. of Stryker Corporation |
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