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

Clearance record K110101

TAPER OXINIUM FEMORAL HEAD · Smith & Nephew, Inc. · decided 2011-04-11 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
OXINIUM71343505Smith & Nephew, Inc.LZO00885556533895
OXINIUM71341904Smith & Nephew, Inc.LZO00885556112540
OXINIUM71341905Smith & Nephew, Inc.LZO00885556112533
OXINIUM71341910Smith & Nephew, Inc.LZO00885556112502
OXINIUM71341940Smith & Nephew, Inc.LZO00885556112441
OXINIUM71341916Smith & Nephew, Inc.LZO00885556112465
OXINIUM71341909Smith & Nephew, Inc.LZO00885556112519
OXINIUM71341941Smith & Nephew, Inc.LZO00885556112434
OXINIUM71341906Smith & Nephew, Inc.LZO00885556112526
OXINIUM71341911Smith & Nephew, Inc.LZO00885556112496
OXINIUM71341914Smith & Nephew, Inc.LZO00885556112489
OXINIUM71343405Smith & Nephew, Inc.LZO00885556533802
OXINIUM71343455Smith & Nephew, Inc.LZO00885556533888
OXINIUM71341939Smith & Nephew, Inc.LZO00885556112458
OXINIUM71341915Smith & Nephew, Inc.LZO00885556112472