Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K781979 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ConMed Linvatec, Ultrapower Burs, Linvatec Corporation, Largo, FL 33773 | 2 | 04/08/2008 | Linvatec Corp. |
Ultra Power Burs, Sterile, Single-Use. | 2 | 10/23/2004 | Linvatec Corp. |
-