Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K983226 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Omnifit Eon These devices are modular components of a total hip system. These femoral stems are i... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
Omnifit FC Cemented Stem These devices are modular components of a total hip system. These femora... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
-