K243890
- 510(k) number
- K243890
- Device name
- Arthrex Intramedullary Nails
- Applicant
- Arthrex, Inc. FL · US
- Product code
- HSB — Rod, Fixation, Intramedullary And Accessories
- Decision date
- 2025-01-13
- Date received
- 2024-12-18
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K243890.pdf
Official FDA record: K243890
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.