Medical Device Recalls
-
|
11 to 11 of 11 Results
510(K) Number: K202924 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Tibial Augment; Item Numbers: (1) 880-331/11 (Sz. 1-2 - cemented x-sm), (2) 880-331/12 (Sz. 1-2 - ce... | 2 | 04/30/2025 | Waldemar Link GmbH & Co. KG (Mfg Site) |
-







