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Thoracic Endovascular Aortic Repair Adverse Events Reported In The Food And Drug Administration Manufacturer And User Facility Device Experience Database
PURPOSE: The purpose of this study is to identify adverse events (device- and patient-related) associated with thoracic aortic stent graft systems and their timing post-procedure. MATERIALS AND METHODS: The Food and Drug Administration’s Manufacturer and User Facility Device Experience (FDA-MAUDE) v...
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| Publicado no: | Med Devices (Auckl) |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6861529/ https://ncbi.nlm.nih.gov/pubmed/31814779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/MDER.S206269 |
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