Medical Device Recalls
-
1 result found
510(K) Number: K092190 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components. | 2 | 06/19/2014 | Synthes, Inc. |
-