ASTM F 1581 : 2008 : R2020
Current
The latest, up-to-date edition.
Standard Specification for Composition of Anorganic Bone for Surgical Implants
Hardcopy , PDF
English
01-09-2020
Committee |
F 04
|
DocumentType |
Standard
|
Pages |
4
|
PublisherName |
American Society for Testing and Materials
|
Status |
Current
|
Supersedes |
1.1This specification covers material requirements for anorganic xenogeneic or allogeneic bone (apatite) intended for surgical implants. For a material to be called anorganic or deorganified bone, it must conform to this specification (see Appendix X1).
1.2The biological response to apatite in soft tissue and bone has been characterized by a history of clinical use and by laboratory studies (1, 2, 3).2 Xenogeneic bone, with organic components present, has been shown to be antigenic in the human host (4) whereas the same material that has been completely deorganified has been shown to elicit no inflammatory or foreign body reactions in human clinical use (5, 6, 7).
1.3This specification specifically excludes synthetic hydroxylapatite, hydroxylapatite coatings, ceramic glasses, tribasic calcium phosphate, whitlockite, and alpha- and beta-tricalcium phosphate.
1.4The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.5Warning—Mercury has been designated by many regulatory agencies as a hazardous substance that can cause serious medical issues. Mercury, or its vapor, has been demonstrated to be hazardous to health and corrosive to materials. Use caution when handling mercury and mercury-containing products. See the applicable product Safety Data Sheet (SDS) for additional information. The potential exists that selling mercury or mercury-containing products, or both, is prohibited by local or national law. Users must determine legality of sales in their location.
1.6This 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. (See Appendix X2).
1.7This 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.
ASTM F 1185 : 2023 | Standard Specification for Composition of Medical-Grade Hydroxylapatite for Surgical Implants |
ASTM D 2972 : 2015 | Standard Test Methods for Arsenic in Water |
ASTM D 3919 : 2015 | Standard Practice for Measuring Trace Elements in Water by Graphite Furnace Atomic Absorption Spectrophotometry (Withdrawn 2024) |
ASTM E 1184 : 2010 : R2016 | Standard Practice for Determination of Elements by Graphite Furnace Atomic Absorption Spectrometry |
ASTM E 1184 : 2021 | Standard Practice for Determination of Elements by Graphite Furnace Atomic Absorption Spectrometry |
ASTM D 513 : 1992 : R1996 | Standard Test Methods for Total and Dissolved Carbon Dioxide in Water |
ASTM D 3559 : 1996 | Standard Test Methods for Lead in Water |
ASTM D 1688 : 1995 | Standard Test Methods for Copper in Water |
ASTM D 2972 : 1997 | Standard Test Methods for Arsenic in Water |
ASTM D 3557 : 1995 | Standard Test Methods for Cadmium in Water |
ASTM F 1185 : 2003 : R2014 | Standard Specification for Composition of Hydroxylapatite for Surgical Implants |
ASTM D 3559 : 2015 | Standard Test Methods for Lead in Water (Withdrawn 2024) |
ASTM D 2972 : 2015 : R2023 | Standard Test Methods for Arsenic in Water |
ASTM E 1184 : 1998 | Standard Practice for Electrothermal (Graphite Furnace) Atomic Absorption Analysis |
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