Medical Device Recalls
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1 result found
510(K) Number: K241470 |
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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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| LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136. | 2 | 04/10/2026 |
FEI # 3006721341 Linkbio Corp. |
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