K243810
- 510(k) number
- K243810
- Device name
- TraumaCad Neo (1.1)
- Applicant
- Brainlab , Ltd. IL
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2025-06-04
- Date received
- 2024-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K243810.pdf
Official FDA record: K243810
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.