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Assessing the use of finite element analysis for mechanical performance evaluation of intervertebral body fusion devices

机译:评估使用有限元分析对椎间体融合装置的机械性能评估

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Background Intervertebral body fusion devices (IBFDs) are a widely used type of spinal implant placed between two vertebral bodies to stabilize the spine for fusion in the treatment of spinal pathologies. Assessing mechanical performance of these devices is critical during the design, verification, and regulatory evaluation phases of development. While traditionally evaluated with physical bench testing, empirical assessments are at times supplemented with computational models and simulations such as finite element analysis (FEA). However, unlike many mechanical bench tests, FEA lacks standardized practices and consistency of implementation. Objectives The objectives of this study were twofold. First, to identify IBFD 510(k) submissions containing FEA and conduct a comprehensive review of the elements provided in the FEA reports. Second, to engage with spinal device manufacturers through an anonymous survey and assess their practices for implementing FEA. Methods First, a retrospective analysis of 510(k) submissions for IBFDs cleared by the FDA between 2013 and 2017 was performed. The contents of FEA test reports were quantified according to FDA guidance. Second, a survey inquiring about the use of FEA was distributed to industry and academic stakeholders. The survey asked up to 20 questions relating to modeler experience and modeling practices. Results Significant gaps were present in model test reports that deemed the data unreliable and, therefore, unusable for regulatory decision‐making in a high percentage of submissions. Nonetheless, the industry survey revealed most stakeholders employ FEA during device evaluation and are interested in more prescriptive guidelines for executing IBFD models. Conclusions This study showed that while inconsistencies and gaps in FEA execution do exist within the spinal device community, the stakeholders are eager to work together in developing standardized approaches for executing computational models to support mechanical performance assessment of spinal devices in regulatory submissions.
机译:背景技术椎体融合装置(IBFD)是置于两个椎体之间的广泛使用的脊柱植入物,以稳定脊柱以融合脊柱病理学。评估这些器件的机械性能在设计,验证和发展的调节阶段至关重要。虽然传统上用物理台阶测试评估,但有时补充有限计算模型和仿真等有限元分析(FEA)的实证评估。但是,与许多机械台阶测试不同,FEA缺乏标准化实践和实施的一致性。目的这项研究的目标是双重的。首先,要识别包含FEA的IBFD 510(k)提交,并对FEA报告中提供的要素进行全面审查。其次,通过匿名调查与脊柱设备制造商进行互动,并评估其实施FEA的实践。方法首先,对2013年至2017年至2017年间FDA清除的510(k)申请的回顾性分析为510(k)已清除的IBFDS。根据FDA指导量化FEA测试报告的内容。其次,对使用FEA的调查被分发给工业和学术利益攸关方。该调查显示了与建模者体验和建模实践有关的20个问题。结果模型试验报告中存在显着差距,认为数据不可靠,因此,对于高百分比提交的监管决策不可用。尽管如此,行业调查显示,大多数利益相关者在设备评估期间雇用FEA,并对执行IBFD模型的更规定的准则感兴趣。结论这项研究表明,虽然FEA执行中的不一致和差距确实存在于脊柱设备社区中,但利益相关者渴望共同开发执行计算模型以支持监管意见中的脊髓设备的机械性能评估的标准化方法。

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