Medical Device Recalls
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1 result found
510(K) Number: K060072 |
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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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OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral c... | 2 | 10/21/2019 | OMNIlife science Inc. |
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