Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K100886 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS | 2 | 12/01/2021 | Wright Medical Technology Inc |
INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS | 2 | 12/01/2021 | Wright Medical Technology Inc |
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