Medical Device Recalls
-
|
1 result found
510(K) Number: K193129 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment ... | 2 | 12/02/2020 |
FEI # 3008599177 K2M, Inc |
-







