Medical Device Recalls
-
1 result found
510(K) Number: K013718 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Gynecare PROLIFT Total Pelvic Repair System PFRT01 Ethicon Deutschland | 2 | 05/10/2007 | Ethicon, Inc. |
-