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Significance and Use
5.1 This test method should be used to evaluate and compare acetabular prostheses to assess the relative degree of constraint for the prosthesis and the damage tolerance under controlled laboratory conditions.
5.2 Although the methodology described attempts to identify physiologically relevant motions and loading conditions, the interpretation of results is limited to an in vitro comparison between acetabular prosthesis designs regarding constraint and their ability to resist impingement fatigue, wear, deformation, and dislocation under the stated test conditions.
1.1 This test method covers a procedure to evaluate acetabular component fatigue, deformation, and wear and femoral head assembly dislocation under dynamic impingement conditions.
1.2 This test method can be used to evaluate single-piece acetabular prostheses, modular prostheses, and constrained prostheses manufactured from polymeric, metallic, or ceramic materials.
1.3 The values stated in SI units are regarded as the standard.
1.4 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
2. Referenced Documents (purchase separately) The documents listed below are referenced within the subject standard but are not provided as part of the standard.
E4 Practices for Force Verification of Testing Machines
E467 Practice for Verification of Constant Amplitude Dynamic Forces in an Axial Fatigue Testing System
F2003 Practice for Accelerated Aging of Ultra-High Molecular Weight Polyethylene after Gamma Irradiation in Air
F2033 Specification for Total Hip Joint Prosthesis and Hip Endoprosthesis Bearing Surfaces Made of Metallic, Ceramic, and Polymeric Materials
F2091 Specification for Acetabular Prostheses
ICS Number Code 11.040.40 (Implants for surgery, prothetics and orthotics)
UNSPSC Code 42321700(Hip joint implants)