ASTM F2996

ASTM F1820

Disassembly forces of modular acetabular devices

ASTM F1875

Fretting corrosion testing of modular implants – Femoral stem-head interface

ASTM F2009

Modular connection disassembly test

ASTM F2068 (PI-98)

Requirements for femoral prostheses - Metallic implants

ASTM F2345

Femoral head fatigue test

ASTM F2580

Fatigue test

ASTM F2582

Impingement test

ASTM F2979

Bearing surface characterization of retrieved hard-on-hard hip prostheses

ASTM F2996

FEA non-modular hip femoral stem

ASTM F3018

Guide for assessment of hard-on-hard articulation THR devices

ASTM F3047M

High demand hip wear testing

ASTM F3090

Fatigue test of acetabular devices

ASTM F3446

3D frictional torque measurement of total hip joint prostheses

ISO 11491

Impact resistance femoral heads

ISO 14242-1

Hip wear test

ISO 14242-1

Third body wear test based on ISO 14242-1

ISO 14242-4

Microseparation test

ISO 21534

Particular requirements for joint replacement implants

ISO 21535

Hip range of motion

ISO 21535

Specific requirements for hip-joint replacement implants

ISO 7206-1

Classification and designation of dimensions

ISO 7206-10

Femoral head compression test

ISO 7206-12

Deformation test for acetabular shells

ISO 7206-13

Femoral head torsion test

ISO 7206-2

Hip surface analysis

ISO 7206-4

Fatigue test

ISO 7206-6

Fatigue test

ISO 7206-8

Fatigue test

PI-11

Insert compression test

PI-3

Luxation test

PI-58 (ISO 7206-8)

Fatigue test

PI-87

FEA non-modular hip femoral stem - neck region

PI-99 (ASTM F2091)

Standard specification for acetabular prostheses

FEA non-modular hip femoral stem

Normative References

ASTM F2996: Standard Practice for Finite Element Analysis (FEA) of Non-Modular Metallic Orthopaedic Hip Femoral Stems

This standard establishes requirements and considerations for developing Finite Element models to evaluate static implant stresses and strains of non-modular metallic orthopaedic hip stem designs. It can be used for worst-case assessment within a family of implant sizes to reduce the need for physical testing. The boundary conditions are set-up according to ISO 7206-4.
The verification and validation of computational models is an essential component for an accurate simulation. To establish model credibility, EndoLab follows the guidelines described in ASME V&V40.

Your contact person

Dipl. Ing. Hugo Hennion

Project Engineer FEA