FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Stealth AXiS™ Surgical System with Stealth AXiS™ Spine clinical application

K Number: K253381 · Decision Feb 12, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
35
Review Days
135

Basic Information

Device Name
Stealth AXiS™ Surgical System with Stealth AXiS™ Spine clinical application
K Number
K253381
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Navigation, Inc.
Date Received
September 30, 2025
Decision Date
February 12, 2026
Product Code
OLO
Advisory Committee
Neurology
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OLO Orthopedic Stereotaxic Instrument

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Other Clearances by Medtronic Navigation, Inc.

K Number Device Name
K253379 Stealth AXiS Cranial clinical application
K253395 Stealth AXiS™ ENT clinical application
K253391 Visualase Cooled Laser Applicator System (9735559); Visualase Cooled Laser Applicator System (9735560); Visualase Cooled Laser Applicator System (9735561)
K251282 StealthStation S8 Spine Software
K242464 Stealth™ Spine Clamps; ModuLeX™ Shank Mounts
K240465 O-arm O2 Imaging System
K231976 StealthStation Cranial Software, v3.1.5 (9735585)
K221087 Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4
K211269 Visualase MRI-Guided Laser Ablation System (SW 3.4)
K203639 StealthStation Cranial Software v1.3.2
Search all 35 clearances from Medtronic Navigation, Inc. →