Medical Device Recalls
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1 result found
510(K) Number: K043048 |
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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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| Medtronic Grafton Plus Paste a) DBM S45001 GRAFTON 1CC PASTE, REF S45001; b) DBM S45005 GRAFTON... | 2 | 04/04/2023 |
FEI # 1000477302 Medtronic Sofamor Danek USA Inc |
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