Medical Device Recalls
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1 result found
510(K) Number: K173832 |
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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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XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use Only, ... | 3 | 11/06/2020 | XTANT Medical |
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