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FDA Regulatory Pathways and Technical Considerations for the 3D Printing of Medical Models and Devices

  • Coburn J
  • Grant G
Springer International Publishing, (2017), 97-111
DOI: 10.1007/978-3-319-61924-8_10
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Coburn, J. C., & Grant, G. T. (2017). FDA Regulatory Pathways and Technical Considerations for the 3D Printing of Medical Models and Devices. In 3D Printing in Medicine (pp. 97–111). Springer International Publishing. https://doi.org/10.1007/978-3-319-61924-8_10

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