1. Scope
1.1 This test method covers in vitro degradation of hydrolytically degradable polymers (HDP) intended for use in surgical
implants. It provides a detailed methodology for conditioning samples and suggests
quantitative techniques for evaluating changes in properties (for example, mass, molar
mass, and mechanical strength) over time.
1.1.1 For many types of HDPs, a correlation has been established between in vitro degradation per this practice and in vivo degradation for unloaded specimens (see X1.1.1).

