Medical Device Recalls
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1 result found
510(K) Number: K091788 |
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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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| Panta Nail, Rx only, Sterile, | 2 | 03/23/2017 |
FEI # 3003418325 Integra LifeSciences Corp. |
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