Medical Device Recalls
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1 result found
510(K) Number: K990032 |
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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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RINGLOC ACETABULAR SYSTEM Self-tapping bone screws, Item numbers 103531, 103533, 103534, 103535 - Pr... | 2 | 12/17/2020 | Biomet, Inc. |
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