Medical Device Recalls
-
1 result found
510(K) Number: K113796 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-Loaded Dril... | 2 | 12/24/2014 | Ebi, Llc |
-