ISO 21535:2023

ISO 21535:2023

July 2023
International standard Current

Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants

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.

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Main informations

Collections

International ISO standards

Publication date

July 2023

Number of pages

29 p.

Reference

ISO 21535:2023

ICS Codes

11.040.40   Implants for surgery, prosthetics and orthotics

Print number

1
Sumary
Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants

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.

Replaced standards (2)
ISO 21535:2007
October 2007
International standard Cancelled
Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants

ISO 21535:2007 provides specific requirements for hip joint replacement implants. With regard to safety, this International Standard specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging, information supplied by the manufacturer, and methods of test.

ISO 21535/A1:2016
November 2016
International standard Cancelled
Amendment 1 to standard ISO 21535:2007

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