The Interconnected Ancestral Network of Hip Arthroplasty Device Approval.
PMID: 34161960 ·
A, j, a, y, , P, r, e, m, k, u, m, a, r, ;, , A, n, d, r, e, w, , Z, h, u, ;, , X, i, a, o, h, a, n, , Y, i, n, g, ;, , C, h, r, i, s, t, i, a, n, , A, , P, e, a, n, ;, , N, e, i, l, , P, , S, h, e, t, h, ;, , M, i, c, h, a, e, l, , B, , C, r, o, s, s, ;, , A, l, e, j, a, n, d, r, o, , G, o, n, z, a, l, e, z, , D, e, l, l, a, , V, a, l, l, e
Publicidade
Resumo
In the United States, the most overwhelming medical devices, including hip arthroplasty devices, are cleared for human use by demonstration of "substantial equivalence" to a predicate, previously approved marketed device. This study examined the predicate approval lineages of modern hip arthroplasty devices. The FDA 510(k) and premarket approval databases were searched to identify all approved hip arthroplasty devices since the database's inception in May 28, 1976. Ancestral predicate lineages w
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.