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Regulation · Permit

FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026)

FDA cleared the Medtronic Stealth AXiS surgical system, the first integrated planning, navigation and robotics platform for spine surgery. Combines preoperative planning, intraoperative navigation, and robotic guidance.

Jurisdiction: United States · Effective 2026-02-13

Machine-readable surfaces

Sources (1)

  1. https://news.medtronic.com/2026-02-13-Medtronic-receives-FDA-clearance-for-Stealth-AXiS-TM-surgical-system,-first-integrated-planning,-navigation-and-robotics-platform-for-spine-surgery · 2026-02-13

Status history

  • In effect · 2026-02-13 · agent-recon

    Initial ingestion

Common questions

What does FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) cover?
FDA cleared the Medtronic Stealth AXiS surgical system, the first integrated planning, navigation and robotics platform for spine surgery. Combines preoperative planning, intraoperative navigation, and robotic guidance.
Where does FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) apply?
FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) is recorded as a permitting requirement applying in United States on the DEPLOY registry.
When did FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) take effect?
FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) is recorded as effective February 13, 2026 on the DEPLOY registry.
Is FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) still in effect?
FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) is currently in effect and applies to covered operators in the named jurisdiction.
What types of robots does FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) apply to?
FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026) is recorded as applying to surgical on the DEPLOY registry.
Which robot models on the DEPLOY registry fall under FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026)?
8 robot models on the DEPLOY registry match the form-factor scope of FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026): ANOVO, Andromeda Surgical Robot, CORI, Carina and 4 others. Form-factor scope match does not by itself establish compliance status; review the underlying primary sources for each operator.
Methodology: Unreviewed · 1 source (no primary) · last reviewed 2026-08-09

Verification posture

Unreviewed

Low confidence

Review state

Stable

Last reviewed 2026-08-09

Architectural position

Cohort: surgical

Sources by quality tier

1
unclassified
Unclassified source

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for FDA 510(k) Clearance: Medtronic Stealth AXiS Surgical System for Spine (Feb 2026).

Canonical ID a0851a8a-a3c6-4ca1-bef2-6a557a289932