Medical Device Recalls
-
1 result found
510(K) Number: K010434 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Optetrak, B-series cemented finned tibial tray size 2f/2t. Catalog # 220-04-02 | 2 | 11/21/2006 | Exactech, Inc. |
-