Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K150890 |
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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 Knee System, Catalog Numbers: a) 02-012-47-3011, b) 02-012-47-5009, c... | 2 | 01/18/2024 | Exactech, Inc. |
Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented to... | 2 | 02/26/2020 | Exactech, Inc. |
Optetrak Logic CC Stem Extension, 22mm x 160mm The OPTETRAK Logic CC Total Knee System is indicat... | 2 | 09/20/2018 | Exactech, Inc. |
Exactech Optetrak Logic CC 15mm Tibial Augment Screws | 2 | 06/19/2017 | Exactech, Inc. |
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