Medical Device Recalls
-
|
1 result found
510(K) Number: K051642 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Artic... | 2 | 03/20/2026 |
FEI # 3004369035 I.T.S. GmbH |
-







