Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K043427 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Suturable DuraGen Dural Regenerative Matrix Suturable DuraGen Dural Regenerative Matrix is an abs... | 2 | 05/10/2013 | Integra LifeSciences Corporation |
Suturable DuraGen Dural Regeneration Matrix; Non-Pyrogenic; Sterility guaranteed unless package is... | 2 | 03/11/2010 | Integra LifeSciences Corp |
-