Medical Device Recalls
-
|
11 to 11 of 11 Results
510(K) Number: K100986 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| ACUMED IMPACT 10CC. Product Number: 65-0110-S, UDI: 813845020269 - Callos is indicated to fill bony... | 2 | 07/15/2020 | Skeletal Kinetics, Llc |
-







