Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120359 |
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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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stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation | 2 | 04/26/2023 | Wright Medical Technology, Inc. |
stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation | 2 | 04/26/2023 | Wright Medical Technology, Inc. |
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