Medical Device Recalls
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1 result found
510(K) Number: K173767 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| A.L.P.S. Clavicle Plating System, Plate, Fixation, Bone, Item Number 233500004 - Product Usage: indi... | 2 | 01/21/2021 |
FEI # 1825034 Biomet, Inc. |
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