Medical Device Recalls
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1 result found
510(K) Number: K182704 |
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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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| WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device. | 2 | 05/10/2024 |
FEI # 3013680140 Wishbone Medical, Inc. |
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