Innovasis received clearance that adds a nano-scale surface designation to three hydroxyapatite-titanium interbody product lines.
- Type
- FDA decision
- Company
- Innovasis
- Device
- AxTiHA stand-alone ALIF, TxTiHA and HAtetracell-C cervical interbody systems
- Date
- 11 September 2026
- Jurisdiction
- US
- Classification
- 510(k) K262025 (OVD)
- Source
- FDA 510(k) database
Official source →Source checked