Medical Device Recalls
-
|
1 result found
510(K) Number: K964880 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Various trauma and sports medicine instruments and implants. Appliance, fixation, nail/blade/plate ... | 2 | 05/26/2016 |
FEI # 1825034 Biomet, Inc. |
-







