Medical Device Recalls
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1 result found
510(K) Number: K972322 |
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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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Sterile Trac System Thinflap 24 MM Burr Hole Plate, Item number SP-STA-1021-12 - Product Usage: Fixa... | 2 | 12/17/2020 | Biomet, Inc. |
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