Medical Device Recalls
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1 to 7 of 7 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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OPTETRAK Three Peg Patella, Item Numbers: a) 200-02-26, 26MM; b) 200-02-29, 29MM; c) 200-02-3... | 2 | 06/18/2024 | Exactech, Inc. |
OPTETRAK Inset Patella, Item Numbers: a) 200-05-23, 23MM; b) 200-05-26, 26MM; c) 200-05-29... | 2 | 06/18/2024 | Exactech, Inc. |
OPTETRAK One Peg Patella,, Item Numbers: a) 200-03-26, 26MM; b) 200-03-29, 29MM; c) 200-03-32... | 2 | 06/18/2024 | Exactech, Inc. |
OPTETRAK, Advanced Patella, 3 Peg Implant, Item Numbers: a) 200-07-26, 26MM; b) 200-07-29, 29MM... | 2 | 06/18/2024 | Exactech, Inc. |
Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d... | 2 | 01/18/2024 | Exactech, Inc. |
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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