Medical Device Recalls
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1 result found
510(K) Number: K052971 |
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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 Trio Small Offset Connector Non Sterile; Manufactured by Stryker Spine SAS, Z.I. Marticot -... | 2 | 04/10/2009 |
FEI # 3004024955 Stryker Spine |
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