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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K020279
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Product Description
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Recall
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FDA Recall
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2.5mm Hex Driver 2 02/27/2004 U&I America
4mm Hex Driver 2 02/27/2004 U&I America
Optima Poly Screw Driver. 2 08/27/2003 U&I America
Optima Spinal System and Spinal Hook System, set screw component. 2 09/08/2004 U&I America
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