Medical Device Recalls
-
|
1 result found
510(K) Number: K140423 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as... | 2 | 12/11/2014 |
FEI # 3009844603 ConforMIS, Inc. |
-







