Medical Device Recalls
-
1 result found
510(K) Number: K140830 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee S... | 2 | 10/26/2015 | Encore Medical, Lp |
-