FDA 510(k) Applications for Medical Device Product Code: JDG (Prosthesis, Hip, Femoral Component, Cemented, Metal)

FDA 510(k) Applications for Medical Device Product Code "JDG"
(Prosthesis, Hip, Femoral Component, Cemented, Metal)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K193546	Biomet Inc.	Distal Centralizers	09/25/2020
K212431	Biomet, Inc.	Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve	02/07/2022
K992234	CORIN U.S.A.	THE TAPER-FIT TOTAL HIP SYSTEM	11/10/1999
K962002	EXACTECH, INC.	AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEM	08/08/1996
K955171	NEXMED, INC.	NEXLOCK FEMORAL STEM	02/09/1996
K001984	STELKAST COMPANY	PROGENY FORGED COCR CEMENTED FEMORAL COMPONENT	09/27/2000
K173499	Stryker Orthopaedics	Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads	03/19/2018