Recalls of Arthroscopic Equipment After Food and Drug Administration 510(k) Approval: A Twenty-Year Analysis of Causes, Trends, and Time to Recall (2004 to 2024)

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Publication Details

Journal
Journal of the American Academy of Orthopaedic Surgeons
Published
2025-09-04
DOI
https://doi.org/10.5435/jaaos-d-25-00371
Primary Topic
Digital Imaging in Medicine
Type
article
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article

Recalls of Arthroscopic Equipment After Food and Drug Administration 510(k) Approval: A Twenty-Year Analysis of Causes, Trends, and Time to Recall (2004 to 2024)

Prem N. Ramkumar, R. Justin Mistovich, Thriaksh Rajan, Comron Saifi et al.
Journal of the American Academy of Orthopaedic Surgeons
Digital Imaging in Medicine
article

Recalls of Arthroscopic Equipment After Food and Drug Administration 510(k) Approval: A Twenty-Year Analysis of Causes, Trends, and Time to Recall (2004 to 2024)

Prem N. Ramkumar, R. Justin Mistovich, Thriaksh Rajan, Comron Saifi, Christian J. Hecht
article en

Abstract

No abstract available for this paper.
Journal of the American Academy of Orthopaedic SurgeonsVol. 34(5)
Cornell University (US), Advisory Board Company (United States) (US), Allied Services (US), Globus Medical (United States) (US), Community Options (United States) (US), Institute of Ethnology (HU), Case Western Reserve University (US), NuVasive (United States) (US)
Openalex Percentile: Top 68%
Digital Imaging in Medicine
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Recalls of Arthroscopic Equipment After Food and Drug Administration 510(k) Approval: A Twenty-Year Analysis of Causes, Trends, and Time to Recall (2004 to 2024) — Prem N. Ramkumar, R. Justin Mistovich, et al. · Journal of the American Academy of Orthopaedic Surgeons (2025) | TGRS Research Map | TGRS