Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K202924 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. ... | 2 | 09/08/2025 |
FEI # 3003386935 Waldemar Link GmbH & Co. KG (Mfg Site) |
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