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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K150241

Genesis II XLPE Resurfacing Patellar Components · Smith & Nephew, Inc. · decided 2015-10-27 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Genesis II71935018Smith & Nephew, Inc.JWH00885556463291
Genesis II71935011Smith & Nephew, Inc.JWH00885556462942
Genesis II71935014Smith & Nephew, Inc.JWH00885556463093
Genesis II71935012Smith & Nephew, Inc.JWH00885556462997
Journey IIE0017873-1Smith & Nephew, Inc.JWH00885556887790
Genesis II71935017Smith & Nephew, Inc.JWH00885556463246
Journey IIE0016670-4Smith & Nephew, Inc.JWH00885556765494
Genesis II71935013Smith & Nephew, Inc.JWH00885556463048
Genesis II71935015Smith & Nephew, Inc.JWH00885556463147
Journey IIE0017575-1Smith & Nephew, Inc.JWH00885556867426
Genesis II71935019Smith & Nephew, Inc.JWH00885556463345
Genesis II71935016Smith & Nephew, Inc.JWH00885556463192