Medical Device Recalls
-
|
1 to 6 of 6 Results
510(K) Number: K072207 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| DuraGen XS Dural Regeneration Matrix: 2 inches x 2 inches. Non Pyrogenic; Rx only;Integra LifeScien... | 2 | 11/24/2010 | Integra LifeSciences Corp. |
| DuraGen XS Dural Regeneration Matrix: 3 inches x 3 inches. Non Pyrogenic; Rx only;Integra LifeScien... | 2 | 11/24/2010 | Integra LifeSciences Corp. |
| DuraGen XS Dural Regeneration Matrix: 4 inches x 5 inches. Non Pyrogenic; Rx only;Integra LifeScien... | 2 | 11/24/2010 | Integra LifeSciences Corp. |
| DuraGen XS Dural Regeneration Matrix: 5 inches x 7 inches. Non Pyrogenic; Rx only;Integra LifeScien... | 2 | 11/24/2010 | Integra LifeSciences Corp. |
| DuraGen XS Dural Regeneration Matrix DuraGen XS Dural Regenerative Matrix is an absorbable implan... | 2 | 05/10/2013 | Integra LifeSciences Corporation |
| NeuraWrap Nerve Protector NeuraWrap Nerve Protector is indicated for the management of peripheral... | 2 | 05/10/2013 | Integra LifeSciences Corporation |
-







