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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: K012314
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Product Description
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FDA Recall
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Smith & Nephew Dyonics Electroblade Resector, 4.5mm Full Radius Blade, BONECUTTER Part Number: 7220... 2 08/03/2012 FEI # 3003604053
Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew 5.5mm DYONICS BONECUTTER ELECTROBLADE Resector Catalog Number: 7205962. 2 01/11/2012 FEI # 3003604053
Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 7205962 Produc... 2 08/03/2012 FEI # 3003604053
Smith & Nephew, Inc. Endoscopy Division
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