Medical Device Recalls
-
|
1 result found
510(K) Number: K072417 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals... | 2 | 01/04/2017 | Smith & Nephew, Inc. |
-







