Medical Device Recalls
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1 result found
510(K) Number: K912190 |
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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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| Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with Break-Away Femoral Noz... | 2 | 07/29/2003 |
FEI # 1811755 Stryker Instruments, Instruments Div. |
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