Medical Device Recalls
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1 result found
510(K) Number: K210935 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix) with the below descriptions a... | 2 | 03/20/2026 |
FEI # 3004369035 I.T.S. GmbH |
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