ISO 6474-2:2019

Implants for surgery — Ceramic materials — Part 2: Composite materials based on a high-purity alumina matrix with zirconia reinforcement

Implants for surgery — Ceramic materials — Part 2: Composite materials based on a high-purity alumina matrix with zirconia reinforcement

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Referenced standards

ASTM C1161ASTM C1198ASTM C1239ASTM C1259ASTM C1327ASTM C1331ASTM C1421ASTM C1499EN 623-2EN 623-3EN 843-1EN 843-2EN 843-4EN 843-5ISO 12677ISO 13356ISO 13383-1ISO 14242-1ISO 14243-1ISO 14704ISO 14705ISO 15732ISO 16428ISO 17561ISO 18754ISO 18756ISO 20501ISO 22214ISO 23146
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ISO 6474-2:2019

Implants for surgery — Ceramic materials — Part 2: Composite materials based on a high-purity alumina matrix with zirconia reinforcement

Implants for surgery — Ceramic materials — Part 2: Composite materials based on a high-purity alumina matrix with zirconia reinforcement

This document specifies the characteristics of, and corresponding test methods for bio-stable ceramic-bone-substitute material based on a zirconia-reinforced, high-purity alumina matrix composite for use as bone spacers, bone replacements and components in orthopaedic joint prostheses.

This document is intended for composite materials which are based on an alumina matrix, i.e. alumina as the dominating phase in the composite with a mass fraction of >60 %, similar to the material described in ISO 6474-1, but extended by means of a certain amount of zirconia and other defined ingredients.

NOTE The required properties in this document differ from those in ISO 6474-1 with respect to strength and fracture toughness. Furthermore, there are requirements specifically applicable for zirconia-containing materials (see ISO 13356).

In the material composition as defined in this document, additional additives are listed. Typical additives for alumina or zirconia ceramics are Mg, Y, Ce and others. Such additives can be useful in order to improve the mechanical properties and/or the chemical stability of the alumina-zirconia composite material.

This document does not cover biocompatibility (see ISO 10993-1). It is the responsibility of the manufacturer to evaluate the biocompatibility of the specific ceramic composite material which is produced within the framework of this document.

Edition2019
Standard Part No2
Published Date2019
Published ByInternational Standardization Organisation
Page Count12