Xenix Medical's RIVA pedicle screw system and RIVA Anchor sacroiliac/spinopelvic fixation were cleared with its NanoACTIV surface treatment on the implants.
- Type
- FDA decision
- Company
- Xenix Medical
- Device
- RIVA Posterior Fixation and RIVA Anchor Sacroiliac Fixation systems with NanoACTIV surface
- Date
- 14 September 2026
- Jurisdiction
- US
- Classification
- 510(k) K262193 (NKB; KWQ, OLO, OUR)
- Source
- FDA 510(k) database
Official source →Source checked