Medical Device Recalls
-
|
1 result found
510(K) Number: K982180 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Dural Graft Matrix DuraGen® Dural Graft Matrix is an absorbable implant for repair of dural defe... | 2 | 05/10/2013 |
FEI # 1121308 Integra LifeSciences Corporation |
-







