Medical Device Recalls
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1 result found
510(K) Number: K070241 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Integra® Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 ... | 2 | 08/01/2012 | Integra LifeSciences Corp. |
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