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Spinal Frontiers · Regulatory Watch · FDA decision

Xenix clears nanotextured surface on RIVA screws and SI anchor

FDA decision · Xenix Medical

14 September 2026

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

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