Medical Device Recalls
-
1 result found
510(K) Number: K083154 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Titanium SURFIX ALPHA SCREWS, a component of the Newdeal Hallu Lock Plate System. Surfix Alpha Varia... | 2 | 03/02/2012 | Integra LifeSciences Corp. |
-