Medical Device Recalls
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1 result found
510(K) Number: K021351 |
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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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| Biosteon brand HA/PLLA Cross Pin, Model Number 234-500-350; Product is distributed by Stryker En... | 3 | 11/18/2005 |
FEI # 2936485 Stryker Endoscopy |
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