Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Nexus Spine

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest FDA decision2026-06-22
TypeNumberDevice NameCodeDateActions
510(k) K261279 DeltaNEC Interbody SystemOVE2026-06-22 View
510(k) K253331 PressON Spinal Fixation SystemNKB2025-10-14 View
↑