Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K063166 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. ... | 2 | 03/20/2026 |
FEI # 3004369035 I.T.S. GmbH |
| Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant tempora... | 2 | 06/04/2019 |
FEI # 3004369035 I.T.S. GmbH |
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