LetterLETTER
Polymer Embolism from Bioactive and Hydrogel Coil Embolization Technology: Considerations for Product Development
A.M. Chopra, J.P. Cruz and Y.C. Hu
American Journal of Neuroradiology May 2019, DOI: https://doi.org/10.3174/ajnr.A6083
A.M. Chopra
aChemical Engineer/Medical Researcher
Camarillo, California
J.P. Cruz
bDepartment of Radiology
Hospital Clínico de la Pontificia Universidad Católica de Chile
Santiago, Chile
Y.C. Hu
cDepartment of Neurosurgery
University Hospitals Cleveland Medical Center
Cleveland, Ohio
REFERENCES
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- Reinges MH,
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- Drexler AY, et al
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- 4.↵U.S. Food and Drug Administration Safety Communications. Lubricious Coating Separation from Intravascular Medical Devices: FDA Safety Communication. November 23, 2015. http://wayback.archive-it.org/7993/20170404182155/https://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm473794.htm. Accessed January 13, 2019
- 5.↵U.S. Food and Drug Administration. Recognized Consensus Standards. Recognition number 3–99, AAMI TIR42:2010. Evaluation of Particulates Associated with Vascular Medical Devices. Updated September 17, 2018. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfStandards/detail.cfm?standard__identification_no=38909. Accessed 13 January 13, 2019
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Polymer Embolism from Bioactive and Hydrogel Coil Embolization Technology: Considerations for Product Development
A.M. Chopra, J.P. Cruz, Y.C. Hu
American Journal of Neuroradiology May 2019, DOI: 10.3174/ajnr.A6083
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