K240172
- 510(k) number
- K240172
- Device name
- Preview Shoulder
- Applicant
- Genesis Software Innovations MI · US
- Product code
- QIH — Automated Radiological Image Processing Software
- Decision date
- 2024-04-04
- Date received
- 2024-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K240172.pdf
Official FDA record: K240172
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.