Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K933610 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Cemented Trapezoid Tibial Tray Sz. 4F/4T, Knee joint patellofemorotibial polymer/metal/polymer semi-... | 2 | 12/23/2004 | Exactech, Inc. |
Product is labeled in part: "***OPTETRAK***TIBIAL TRAY***TRAPEZOID CEMENTED***Ti Alloy*** SIZE 1F/1... | 2 | 07/24/2012 | Exactech, Inc. |
Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d... | 2 | 01/18/2024 | Exactech, Inc. |
-