Medical Device Recalls
-
1 result found
510(K) Number: K132161 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
OPTETRAK LOGIC Polyethylene Tibial Inserts, labeled as the following: a. OPTETRAK Logic PS Tibi... | 2 | 10/04/2021 | Exactech, Inc. |
-