Medical Device Recalls
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1 result found
510(K) Number: K163489 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SYSTEM 26. Part Numbers: OS900035-NS; OS900036-NS; OS900037-NS; OS900038-NS; OS900040-NS; OS90... | 2 | 03/09/2018 |
FEI # 3008951116 ORTHO SOLUTIONS, LTD. |
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