FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody

K Number: K254157 · Decision May 26, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
96
Review Days
155

Basic Information

Device Name
CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody
K Number
K254157
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medos International SARL
Date Received
December 22, 2025
Decision Date
May 26, 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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