Medical Device Recalls
-
11 to 11 of 11 Results
510(K) Number: K012911 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
LOCATOR Restorative Abutment, ILOA002, LOT 877423, Certain LOCATOR ABUTMENT, 4.1 mm(D) X 2mm(H), STE... | 2 | 02/22/2010 | Biomet 3i, LLC |
-