Medical Device Recalls
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1 result found
510(K) Number: K230202 |
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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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| Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI... | 2 | 03/20/2024 | Think Surgical, Inc. |
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