Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K024161 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W... | 2 | 03/11/2019 |
FEI # 3005751028 Zimmer Trabecular Metal Technology, Inc. |
| NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W... | 2 | 03/11/2019 |
FEI # 3005751028 Zimmer Trabecular Metal Technology, Inc. |
-







