ASTM F 1714 : 1996 : R2013
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Standard Guide for Gravimetric Wear Assessment of Prosthetic Hip Designs in Simulator Devices
Hardcopy , PDF
31-08-2020
English
15-03-2013
CONTAINED IN VOL. 13.01, 2015 Covers a laboratory method using a weight-loss technique for evaluation of wear properties of material or devices, or both, which are being considered for use as bearing surfaces of human-hip-joint replacement prostheses.
Committee |
F 04
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DocumentType |
Guide
|
Pages |
8
|
ProductNote |
Reconfirmed 2013
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PublisherName |
American Society for Testing and Materials
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Status |
Superseded
|
SupersededBy | |
Supersedes |
1.1This guide describes a laboratory method using a weight-loss technique for evaluating the wear properties of materials or devices, or both, which are being considered for use as bearing surfaces of human-hip-joint replacement prostheses. The hip prostheses are evaluated in a device intended to simulate the tribological conditions encountered in the human hip joint, for example, use of a fluid such as bovine serum, or equivalent pseudosynovial fluid shown to simulate similar wear mechanisms and debris generation as found in vivo, and test frequencies of 1 Hz or less.
1.2Since the hip simulator method permits the use of actual implant designs, materials, and physiological load/motion combinations, it can represent a more physiological simulation than basic wear-screening tests, such as pin-on-disk (see Practice F732) or ring-on-disk (see ISO 6474).
1.3It is the intent of this guide to rank the combination of implant designs and materials with regard to material wear-rates, under simulated physiological conditions. It must be recognized, however, that there are many possible variations in the in vivo conditions, a single laboratory simulation with a fixed set of parameters may not be universally representative.
1.4The reference materials for the comparative evaluation of candidate materials, new devices, or components, or a combination thereof, shall be the wear rate of extruded or compression-molded, ultra-high molecular weight (UHMW) polyethylene (see Specification F648) bearing against standard counter faces [stainless steel (see Specification F138); cobalt-chromium-molybdenum alloy (see Specification F75); thermomechanically processed cobalt chrome (see Specification F799); alumina ceramic (see Specification F603)], having typical prosthetic quality, surface finish, and geometry similar to those with established clinical history. These reference materials will be tested under the same wear conditions as the candidate materials.
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ASTM F 2091 : 2015 | Standard Specification for Acetabular Prostheses (Withdrawn 2023) |
ASTM F 2977 : 2013 | Standard Test Method for Small Punch Testing of Polymeric Biomaterials Used in Surgical Implants |
ASTM F 2759 : 2011 | Standard Guide for Assessment of the Ultra High Molecular Weight Polyethylene (UHMWPE) Used in Orthopedic and Spinal Devices |
ASTM F 1877 : 2016 | Standard Practice for Characterization of Particles |
ASTM F 2694 : 2016 | Standard Practice for Functional and Wear Evaluation of Motion-Preserving Lumbar Total Facet Prostheses |
ASTM F 2003 : 2002 : R2015 | Standard Practice for Accelerated Aging of Ultra-High Molecular Weight Polyethylene after Gamma Irradiation in Air |
ASTM F 2025 : 2006 : R2018 | Standard Practice for Gravimetric Measurement of Polymeric Components for Wear Assessment |
ASTM F 2423 : 2011 : R2016 | Standard Guide for Functional, Kinematic, and Wear Assessment of Total Disc Prostheses |
ASTM F 2789 : 2010 : R2015 | Standard Guide for Mechanical and Functional Characterization of Nucleus Devices |
ASTM F 2624 : 2012 : R2016 | Standard Test Method for Static, Dynamic, and Wear Assessment of Extra-Discal Single Level Spinal Constructs |
ASTM F 86 : 2013 : REDLINE | Standard Practice for Surface Preparation and Marking of Metallic Surgical Implants |
ASTM F 565 : 2004 : R2009 | Standard Practice for Care and Handling of Orthopedic Implants and Instruments |
ASTM F 136 : 2013 : REDLINE | Standard Specification for Wrought Titanium-6Aluminum-4Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications (UNS R56401) |
ASTM F 370 : 1994 : R1999 | Standard Specification for Proximal Femoral Endoprosthesis (Withdrawn 2005) |
ASTM F 732 : 2017 : REDLINE | Standard Test Method for Wear Testing of Polymeric Materials Used in Total Joint Prostheses |
ISO 6474:1994 | Implants for surgery Ceramic materials based on high purity alumina |
ASTM F 799 : 2011 : REDLINE | SPECIFICATION FOR COBALT-28CHROMIUM-6MOLYBDENUM ALLOY FORGINGS FOR SURGICAL IMPLANTS (UNS R31537, R31538, R31539) |
ASTM F 648 : 2014 : REDLINE | Standard Specification for Ultra-High-Molecular-Weight Polyethylene Powder and Fabricated Form for Surgical Implants |
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