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

EUROPA™ Posterior Cervical Fusion Navigated Instruments

K Number: K253444 · Decision Mar 18, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
24
Review Days
167

Basic Information

Device Name
EUROPA™ Posterior Cervical Fusion Navigated Instruments
K Number
K253444
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MiRus, LLC
Date Received
October 2, 2025
Decision Date
March 18, 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 MiRus, LLC

K Number Device Name
K252733 ATLAS™ Expandable Osteotomy Wedge System
K242516 EUROPA™ Posterior Cervical Fusion System
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K232348 RIGEL™ 3DR Standalone Anterior Cervical Interbody Fusion System
K232481 RIGEL™ 3DR Anterior Cervical Corpectomy System
K232154 MiRus 3DR Lateral Lumbar Interbody Fusion System with Integrated Plate Fixation
K230369 EUROPA™ Navigated Instruments
K220441 CYGNUS™ MoRe Anterior Cervical Plate System
K220115 ANTARES 3DR Standalone Anterior Lumbar Interbody Fusion System
K210800 IO Expandable Lumbar Interbody Fusion System
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