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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K150818
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Product Description
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Recall
Class
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FDA Recall
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VersaFx Femoral Fixation System Hex head compression screw 4.7 mm dia. 2 inch (51 mm) length 471... 2 05/16/2016 FEI # 1000132037
Zimmer Manufacturing B.V.
Product 31 consists of all product under product code: KTT and same usage: Item no: 118113003 FR... 2 03/12/2016 FEI # 1000132037
Zimmer Manufacturing B.V.
Product 65 consists of all product under product code: KTT and same usage: Item no: 119413594 VER... 2 03/12/2016 FEI # 1000132037
Zimmer Manufacturing B.V.
Product 20 consists of all prod oct under poduct code: KTT and same usage: Item no: 47116201900 ... 2 03/12/2016 FEI # 1000132037
Zimmer Manufacturing B.V.
Product 41 consists of all product under product code: KTT and same usage: Item no: 119301042 LA... 2 03/12/2016 FEI # 1000132037
Zimmer Manufacturing B.V.
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