Medical Device Recalls
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1 result found
510(K) Number: K101100 |
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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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GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only ST... | 2 | 07/01/2013 | Linvatec Corp. dba ConMed Linvatec |
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