This standard is issued under the fixed designation F1814; the number immediately following the designation indicates the year of original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A superscript epsilon (ε) indicates an editorial change since the last revision or reapproval.

1. Scope

1.1

This guide covers a procedure to assist the developer of a modular joint replacement implant in the choice of appropriate tests and evaluations to determine device safety.

1.2

This guide does not attempt to define all test methods associated with modular device evaluation.

1.3

The disassembly testing in this guide does not cover intentional intraoperative disassembly but is meant only to suggest testing necessary to determine inadvertent disassembly loads.

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, health, and environmental practices and determine the applicability of regulatory limitations prior to use.

1.5

This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

2. Referenced Documents

2.1 ASTM Standards:2

2.2 ISO Standards:3

3. Terminology

3.1 Definitions of Terms Specific to This Standard:

4. Significance and Use

4.1

4.2

4.3

4.4

5. Testing

5.1 Assembly

5.2 Disassembly

5.3 Cyclic Fatigue Properties

6. Keywords

6.1

ASTM F1814 - 22

Standard Guide for Evaluating Modular Hip and Knee Joint Components

Current

Published:

15 Jul 2022