Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K181026 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur) | 2 | 11/06/2020 | Merete Medical GmbH |
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus) | 2 | 11/06/2020 | Merete Medical GmbH |
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia) | 2 | 11/06/2020 | Merete Medical GmbH |
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