ASTM F 981 Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
 |
| Purchase Information |
| Use this form to request purchase information on ASTM online subscriptions. |
|
 |
Document ASTM F 981 is offered by IHS as part of an online subscription. This subscription contains many documents on the same topic.
You may also purchase this document alone from the IHS Standards Store.
ASTM F 981 Document Information:
Title
Standard Practice for Assessment of Compatibility of Biomaterials for Surgical Implants with Respect to Effect of Materials on Muscle and Bone
ASTM International
Publication Date:
May 1, 2004
Scope:
This practice provides a series of experimental protocols for
biological assays of tissue reaction
to nonabsorbable biomaterials for surgical implants. It assesses the
effects of the material on
animal tissue in which it is implanted. The experimental protocol is
not designed to provide a
comprehensive assessment of the systemic toxicity, immune response,
carcinogenicity,
teratogenicity, or mutagenicity of the material since other standards
deal with these issues. It
applies only to materials with projected applications in humans where
the materials will reside in
bone or soft tissue in excess of 30 days and will remain unabsorbed.
It is recommended that
short-term assays, according to Practice F 763, first be performed.
Applications in other organ
systems or tissues may be inappropriate and are therefore excluded.
Control materials will consist
of any one of the metal alloys in Specifications F 67, F 75, F 90, F
136, F 138, or F 562, high
purity dense aluminum oxide as described in Specification F 603, ultra
high molecular weight
polyethylene as stated in Specification F 648 or USP polyethylene
negative control.
This practice is a combination of Practice F 361 - 80 and Practice F
469 - 78. The purpose, basic
procedure, and method of evaluation of each type of material are
similar; therefore, they have been
combined.
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.
Keywords:
- biocompatibility
- bone implant materials
- cellular reaction
- histology/histopathology
- implants muscle
- New Zealand rabbits
- orthopaedic medical devices - bone
- plastic surgical devices/applications
- polyethylene (PE) - surgical implant applications
- rabbits
- rats
- scar
- test animals
- tissue compatibility
- tissue response evaluation
About IHS
IHS (NYSE: IHS) is a leading global provider of critical technical information, decision-support tools and related services in a number of industries including aerospace and defense, automotive, construction, electronics, and energy. IHS serves customers ranging from large governments and multinational corporations to smaller companies and technical professionals in more than 100 countries. IHS been in business for more than 45 years and employ more than 2,300 people around the world.