COMPANY
Nexus Spine
Timeline
- FDA FDA 510(k) clearance: DeltaNEC Interbody System — K261279, Jun 22, 2026. Applicant at approval: Nexus Spine. source ↗
- FDA FDA 510(k) clearance: PressON Spinal Fixation System — K253331, Oct 14, 2025. Applicant at approval: Nexus Spine. source ↗
- FDA FDA 510(k) clearance: Stable-L Lumbar Interbody System — K243934, Apr 30, 2025. Applicant at approval: Nexus Spine, LLC. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: DeltaNEC Interbody System — K261279, Jun 22, 2026. Applicant at approval: Nexus Spine. source ↗
- FDA 510(k) clearance: PressON Spinal Fixation System — K253331, Oct 14, 2025. Applicant at approval: Nexus Spine. source ↗
- FDA 510(k) clearance: Stable-L Lumbar Interbody System — K243934, Apr 30, 2025. Applicant at approval: Nexus Spine, LLC. source ↗
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