Original article title
Food and Drug Administration authorization of spine surgery devices: a 2-decade analysis of clearance trends, regulatory pathways, and market entry.
Abstract conclusion
“Regulatory pathway, device class, sponsor experience, and manufacturer location were each associated with time to FDA decision.”
Keep in mind
Research · assess methods and limitations.
pubmed.ncbi.nlm.nih.gov · Full-text access depends on the publisher.
The excerpt is quoted from source text. The original title is preserved above.
This is a reading aid. Follow the source for methods, limitations, corrections, and clinical context.