Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

PubMed

United States regulatory approval of medical devices used for endovascular neurosurgery: A two-decade review of FDA regulatory files.

PMID: 37923383 ·

L, o, k, e, s, h, w, a, r, , S, , B, h, e, n, d, e, r, u, ;, , T, r, e, v, o, r, , H, a, r, d, i, g, a, n, ;, , J, o, r, g, e, , R, o, a, ;, , B, r, a, n, d, o, n, , D, , P, h, i, l, b, r, i, c, k, ;, , A, l, e, x, , H, o, a, n, g, ;, , A, m, i, r, , H, , F, a, r, a, j, i, ;, , G, a, v, i, n, , W, , B, r, i, t, z, ;, , K, u, r, t, , A, , Y, a, e, g, e, r

RevistaJournal of neurointerventional surgery
Año
PMID37923383

Resumen

The evolution of neuroendovascular technologies has progressed substantially. Over the last two decades, the introduction of new endovascular devices has facilitated treatment for more patients, and as a result, the regulatory environment concerning neuroendovascular devices has evolved rapidly in response. To examine trends in the approval of neuroendovascular devices by the United States Food and Drug Administration (FDA) over the last 20 years. Open-access US FDA databases were queried betwee

Fuente oficial

Ver en PubMed →

Datos obtenidos de PubMed / NCBI. Para consultar el texto completo y la información más reciente, remítase siempre al registro oficial.

↑