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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K032945
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1. AutoPlex System, Product Number: 0605-887-000, UDI: (01)4546540593108; 2. AutoPlex System: w/ Ver... 2 03/28/2018 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
Stryker PCD Precision System 13G Needle with Spineplex, sterile, single use, disposable , 4 units pe... 2 01/25/2012 FEI # 1811755
Stryker Instruments Div. of Stryker Corporation
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