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

Shoulder arthroplasty device clearance: an ancestral network analysis.

PMID: 36279987 ·

A, n, d, r, e, w, , Z, h, u, ;, , X, i, a, o, h, a, n, , Y, i, n, g, ;, , E, d, w, a, r, d, , G, , C, a, r, e, y, ;, , C, h, r, i, s, t, i, a, n, , A, , P, e, a, n, ;, , A, j, a, y, , P, r, e, m, k, u, m, a, r, ;, , M, i, c, h, a, e, l, , C, , F, u, ;, , S, a, m, u, e, l, , A, , T, a, y, l, o, r

RevistaJournal of shoulder and elbow surgery
Año
PMID36279987

Resumen

The US Food and Drug Administration (FDA) oversees medical device regulation and oversight in the United States, and the majority of shoulder arthroplasty devices are cleared via the 510(k) pathway, in which a device demonstrates "substantial equivalence" to a previously cleared predicate. The purpose of this study was to determine an interconnected ancestral network of shoulder arthroplasty devices and determine equivalency ties to devices subsequently recalled by the FDA for design-related iss

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.

↑