Medical Device Recalls
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1 result found
510(K) Number: K023409 |
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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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Various Hip systems, Item Nos. 104207 104212 104215 11-162809 11-162810 11-162811 11-162812 1... | 2 | 11/22/2019 | Zimmer Biomet, Inc. |
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