CKI (ClaroNav Kolahi Inc.) has received FDA 510(k) clearance for Navient in ENT procedures, expanding its previous clearance for cranial applications. Navient is now approved by major global regulatory bodies, including Canada (HC), Europe (EU MDD), China (NMPA), UAE, Saudi (SFDA), Taiwan (TFDA), Mexico (Cofepris), Australia (TGA), Colombia (Invima), Peru, Turkey….
Navient is an innovative image-guided navigation system that utilises the latest technologies in surgical navigation systems and brings simplicity, accuracy and affordability to the cranial, spine and ENT navigation systems.
Key Features
General features:
- Supports spine, cranial, biopsy and ENT procedures
- Sleek, compact and portable cart
- Large touch screen for natural interaction
- Powerful and intuitive software features
- Pre-calibrated navigation probes
Spine features:
- 2D and 3D C-arm integration for automatic registration
- Automatic registration using intra-op CT and C-arm
- Endoscopic spine navigation
- AI-powered automatic spine segmentation
Cranial and ENT features
- Navient AIR Touchless registration
- Tractography and advanced cranial planning
- Navigated biopsy and shunt placement
FURTHER INFORMATION:
ClaroNav Kolahi Inc. (CKI)
T: + 1 (647) 951 1525
E: info@claronav.com
W: https://medical.claronav.com/
