K243375
- 510(k) number
- K243375
- Device name
- Ruthless Spine RJB
- Applicant
- Ruthless, LLC Dba Ruthless Spine CA · US
- Product code
- QWL — Intraoperative Surgical Angle Measurement Tool
- Decision date
- 2024-11-29
- Date received
- 2024-10-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K243375.pdf
Official FDA record: K243375
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.