Medical Device Recalls
-
|
1 result found
510(K) Number: K111723 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| ev3 TurboHawk PERPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE, LARGE VESSEL XTENDED TIP FOR CALCIU... | 2 | 09/11/2018 |
FEI # 3004904811 Micro Therapeutics Inc, Dba Ev3 Neurovascular |
-







