K250920
- 510(k) number
- K250920
- Device name
- Arthrex Spine Compression FT Screw
- Applicant
- Arthrex, Inc. FL · US
- Product code
- MRW — System, Facet Screw Spinal Device
- Decision date
- 2025-05-22
- Date received
- 2025-03-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250920.pdf
Official FDA record: K250920
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.