Device details
FDA 510(k) registration fields
- K number
- K231184
- Device name
- CD Horizon™ Spinal System
- Country / Region
- United States(US)
- Product code
- OLO
- Device class
- Class 2
- Regulation number
- 21 CFR 882.4560
- Date received
- 2023-04-26
- Decision date
- 2023-05-26
- Submission type
- Special
- Technology type
- Stereotactic Surgery(AI inferred)
- Clinical applications
- Spine SurgeryNavigation System
- Primary application
- Spine Surgery
- Classification source
- AI classified
