Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932776 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The product is a Finned Tibial Tray. Product is labeled in part: ''OPTETRAK FINNED TIBIAL TRAY A/P... | 2 | 08/18/2005 | Exactech, Inc. |
| Product is Optetrak Cemented Finned Tibial Tray Sz. 4F/5T. Knee prosthesis. Product is labeled in ... | 2 | 06/02/2006 | Exactech, Inc. |
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