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

SPINEART Navigation Instrument System

K Number: K242933 · Decision Jun 18, 2025
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
8
Review Days
266

Basic Information

Device Name
SPINEART Navigation Instrument System
K Number
K242933
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spineart SA
Date Received
September 25, 2024
Decision Date
June 18, 2025
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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