COMPANY

Nexus Spine

Profile checked Oct 10, 2026

Timeline

Jun 22, 2026 FDA FDA 510(k) clearance: DeltaNEC Interbody System — K261279, Jun 22, 2026. Applicant at approval: Nexus Spine. source ↗
Oct 14, 2025 FDA FDA 510(k) clearance: PressON Spinal Fixation System — K253331, Oct 14, 2025. Applicant at approval: Nexus Spine. source ↗
Apr 30, 2025 FDA FDA 510(k) clearance: Stable-L Lumbar Interbody System — K243934, Apr 30, 2025. Applicant at approval: Nexus Spine, LLC. source ↗

Jun 22, 2026 FDA 510(k) clearance: DeltaNEC Interbody System — K261279, Jun 22, 2026. Applicant at approval: Nexus Spine. source ↗
Oct 14, 2025 FDA 510(k) clearance: PressON Spinal Fixation System — K253331, Oct 14, 2025. Applicant at approval: Nexus Spine. source ↗
Apr 30, 2025 FDA 510(k) clearance: Stable-L Lumbar Interbody System — K243934, Apr 30, 2025. Applicant at approval: Nexus Spine, LLC. source ↗

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LinkedIn page linked from the company's own site: source · seen 2026-10-12