Resumen
This document specifies requirements for hip-joint replacement implants. With regard to safety, this document specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging, information supplied by the manufacturer and methods of test.
This document applies to both total and partial hip joint replacement implants. It applies to components made of metallic and non-metallic materials.
This document applies to a wide variety of hip replacement implants, but for some specific hip replacement implant types, some considerations, not specifically covered in this document, can be applicable. Further details are given in 7.2.1.2.
The requirements which are specified in this document are not intended to require the re-design or re-testing of implants which have been legally marketed and for which there is a history of sufficient and safe clinical use. For such implants, compliance with this document can be demonstrated by providing evidence of the implant’s sufficient and safe clinical use.
Preview
Informaciones generales
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Estado: PublicadoFecha de publicación: 2023-07Etapa: Norma Internacional publicada [60.60]
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Edición: 3Número de páginas: 27
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Comité Técnico :ISO/TC 150/SC 4ICS :11.040.40
- RSS actualizaciones
Ciclo de vida
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Anteriormente
RetiradaISO 21535:2007
RetiradaISO 21535:2007/Amd 1:2016
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Ahora
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