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

Ion-C Navigation Instruments

K Number: K260329 · Decision May 22, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
25
Review Days
112

Basic Information

Device Name
Ion-C Navigation Instruments
K Number
K260329
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SurGenTec, LLC
Date Received
January 30, 2026
Decision Date
May 22, 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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K243580 GraftGun Universal Graft Delivery System (GDS)
K243835 TiLink-P SI Joint Fusion System
K242797 OsteoFlo HydroFiber
K243265 Ion 3D
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