Medical Device Recalls
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1 result found
510(K) Number: K143188 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 3.0mm Cannulated Screw System, BCS Cannulated Screw System (3.0, 4.0/5.0, 6.5/8.0mm), Item numbers 1... | 2 | 12/17/2020 |
FEI # 1825034 Biomet, Inc. |
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