Medical Device Recalls
-
1 result found
510(K) Number: K230653 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, ... | 2 | 09/20/2023 | Smith & Nephew Inc |
-