Medical Device Recalls
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1 result found
510(K) Number: K130390 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, ... | 2 | 12/17/2020 |
FEI # 1825034 Biomet, Inc. |
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