Medical Device Recalls
-
1 result found
510(K) Number: K040267 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Triathlon Total Knee System Primary Tibial Baseplate; Sterile, Made in Ireland. Howmedica Osteoni... | 2 | 08/31/2010 | Stryker Howmedica Osteonics Corp. |
-