Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K933610 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Product is labeled in part: "***OPTETRAK***TIBIAL TRAY***TRAPEZOID CEMENTED***Ti Alloy*** SIZE 1F/1... | 2 | 07/24/2012 | Exactech, Inc. |
Cemented Trapezoid Tibial Tray Sz. 4F/4T, Knee joint patellofemorotibial polymer/metal/polymer semi-... | 2 | 12/23/2004 | Exactech, Inc. |
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