Medical Device Recalls
-
|
1 result found
510(K) Number: K070946 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, ... | 2 | 06/10/2016 | Synthes (USA) Products LLC |
-







