Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K062998 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item n... | 2 | 12/04/2018 | Zimmer Biomet, Inc. |
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