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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K092508
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Product Description
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FDA Recall
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Smith & Nephew FAST FIX 360, STRAIGHT NEEDLE Catalog Number; 72202467. Intended for use as a su... 2 11/18/2010 FEI # 3003604053
Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew FAST FIX 360, REVERSE CURVED NEEDLE Catalog Number; 72202469. Intended for use a... 2 11/18/2010 FEI # 3003604053
Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew FAST FIX 360, CURVED NEEDLE Catalog Number; 72202468. Intended for use as a sutu... 2 11/18/2010 FEI # 3003604053
Smith & Nephew, Inc. Endoscopy Division
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