Medical Device Recalls
-
1 result found
510(K) Number: K932519 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Omnifit Normalized Hip Stem These devices are modular components of a total hip system. These fem... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
-