Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K933494 |
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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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Polyethylene tibial posterior stabilized components. Optetrak All Poly Tibial PS Component. Knee pro... | 2 | 02/27/2007 | Exactech, Inc. |
OPTETRAK Comprehensive Knee System, labeled as the following: a. OPTETRAK All-polyethylene CR Ti... | 2 | 10/04/2021 | Exactech, Inc. |
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