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ASTM F2901-13

Historical Revision

Standard Guide for Selecting Tests to Evaluate Potential Neurotoxicity of Medical Devices

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1.1 Medical devices may cause adverse effects on the structure and/or function of the nervous system. In this guide, these adverse effects are defined as neurotoxicity. This guide provides background information and recommendations on methods for neurotoxicity testing. This guide should be used with Practice F748, and may be helpful where neurotoxicity testing is needed to evaluate medical devices that contact nervous system tissue or cerebral spinal fluid (CSF).

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


4.1 The objective of this guide is to recommend a panel of biological tests that can be used in addition to the testing recommended in Practice F748. This guide is designed to detect neurotoxicity caused by medical devices that contact nervous tissue.

4.2 The testing recommendations should be considered for new materials, established materials with different manufacturing methods that could affect nervous tissue response, or materials used in new nervous tissue applications.

4.3 Chemical characterization can be used to evaluate similarity for materials with a history of clinical use in a similar nervous tissue application.

SDO ASTM: ASTM International
Document Number F2901
Publication Date Feb. 1, 2013
Language en - English
Page Count 3
Revision Level 13
Supercedes
Committee F04.16
Publish Date Document Id Type View
March 1, 2019 F2901-19 Revision
Feb. 1, 2013 F2901-13 Revision
Sept. 1, 2012 F2901-12 Revision