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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K094017
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Product Description
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FDA Recall
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Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. The Apex Kn... 2 09/13/2012 FEI # 3008342029
Omni Life Science
Omnilife Science Apex Knee System Modular Tibia Augment, Size 2 x 4mm Ref: KC-54020. The Apex Kn... 2 09/13/2012 FEI # 3008342029
Omni Life Science
Omnilife Science Apex Knee System Modular Tibia Augment, Size 6 x 4mm Ref: KC-54060. The Apex Kn... 2 09/13/2012 FEI # 3008342029
Omni Life Science
Omnilife Science Apex Knee System Modular Tibia Augment, Size 4 x 4mm Ref: KC-54040. The Apex Kn... 2 09/13/2012 FEI # 3008342029
Omni Life Science
Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. The Apex Kn... 2 09/13/2012 FEI # 3008342029
Omni Life Science
Omnilife Science Apex Knee System Modular Tibia Augment, Size 3 x 4mm Ref: KC-54030. The Apex Kn... 2 09/13/2012 FEI # 3008342029
Omni Life Science
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