Device details
FDA 510(k) registration fields
- K number
- K231886
- Device name
- SURGIVISIO Device
- Company
- Ecential Robotics
- Country / Region
- France(FR)
- Product code
- OLO
- Device class
- Class 2
- Regulation number
- 21 CFR 882.4560
- Date received
- 2023-06-27
- Decision date
- 2023-07-27
- Submission type
- Special
- Technology type
- Image Guided Surgery(AI inferred)
- Clinical applications
- Spine SurgeryNavigation SystemOther
- Primary application
- Spine Surgery
- Classification source
- AI classified
