Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K202924 |
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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| LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cement... | 2 | 06/01/2023 | Linkbio Corp. |
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