Reported Events Associated With Spine Robots: An Analysis of the Food and Drug Administration's Manufacturer and User Facility Device Experience Database.
PMID: 36074993 ·
G, r, e, g, o, r, y, , J, , K, i, r, c, h, n, e, r, ;, , A, n, d, r, e, w, , H, , K, i, m, ;, , A, r, i, e, l, , H, , K, w, a, r, t, ;, , J, o, h, n, , B, , W, e, d, d, l, e, ;, , J, e, s, s, e, , E, , B, i, b, l, e
Publicidade
Resumo
Cross-Sectional Analysis. To summarize medical device reports (MDRs) between August 1, 2017 and November 30, 2021 relating to robot-assisted spine systems within the Manufacturer and User Facility Device Experience (MAUDE) database maintained by The Food and Drug Administration (FDA). The MAUDE database was abstract for all MDRs relating to each FDA-approved robot-assisted spine system. Event descriptions were reviewed and characterized into specific event types. Outcome measures include specifi
Publicidade
Fonte oficial
Ver no PubMed →Dados provenientes do PubMed / NCBI. Para consultar o texto integral e as informações mais recentes, recorra sempre ao registo oficial.