Medical Device Recalls
-
|
1 result found
510(K) Number: K032187 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Tibial Opening Wedge Osteotomy Plate, Titanium, 15.0 mm - Product Usage: use in treatment of non-uni... | 2 | 04/09/2021 | Arthrex, Inc. |
-







