Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K033883 |
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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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Exactech Optetrak Logic PS Knee System, Catalog Numbers: 02-012-35-5009 | 2 | 01/18/2024 | Exactech, Inc. |
OPTETRAK LOGIC Polyethylene Tibial Inserts, labeled as the following: a. OPTETRAK Logic PS Tibi... | 2 | 10/04/2021 | Exactech, Inc. |
Optetrak Asymmetric Hi-Flex Posterior Stabilized Cemented Femorals, size 3, Catalog #244-02-03, Cata... | 2 | 01/05/2015 | Exactech, Inc. |
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