K252615
- 510(k) number
- K252615
- Device name
- Ruthless Spine RJB
- Applicant
- Ruthless, LLC Dba Ruthless Spine CA · US
- Product code
- QWL — Intraoperative Surgical Angle Measurement Tool
- Decision date
- 2025-09-17
- Date received
- 2025-08-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K252615.pdf
Official FDA record: K252615
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.