Medical Device Recalls
-
|
1 result found
510(K) Number: K811101 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Zimmer Dental Calcitite 4060-2 Dense Nonresorbable Hydroxylapatite Bone Grafting Material, 4 ampules... | 2 | 02/06/2009 |
FEI # 1000220733 Zimmer Inc. |
-







