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
Anzeige
Zusammenfassung
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
Anzeige
Offizielle Quelle
Auf PubMed ansehen →Daten aus PubMed / NCBI. Den Volltext und die aktuellsten Informationen finden Sie stets im offiziellen Eintrag.