Risk of Recall Among Medical Devices Undergoing US Food and Drug Administration 510(k) Clearance and Premarket Approval, 2008-2017.
PMID: 33956132 ·
J, o, n, a, t, h, a, n, , R, , D, u, b, i, n, ;, , S, t, e, p, h, e, n, , D, , S, i, m, o, n, ;, , K, i, r, s, t, e, n, , N, o, r, r, e, l, l, ;, , J, a, c, o, b, , P, e, r, e, r, a, ;, , J, a, c, o, b, , G, o, w, e, n, ;, , A, k, i, n, , C, i, l
Реклама
Аннотация
The US Food and Drug Administration (FDA) uses 510(k) clearance and premarket approval (PMA) pathways to ensure device safety before marketing. Premarket approval evaluates high-risk medical devices and requires clinical trials, whereas 510(k) clearance evaluates moderate-risk devices and relies on benchtop (nonclinical and biomechanical) and descriptive data. Existing literature suggests that the clinical trials required by PMA are associated with reduced risk of recall compared with devices gr
Реклама
Официальный источник
Открыть в PubMed →Данные получены из PubMed / NCBI. Полный текст и наиболее актуальную информацию всегда смотрите в официальной записи.