FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

ARIX Femur Nail System

K Number: K252826 · Decision Dec 10, 2025
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
53
Review Days
96

Basic Information

Device Name
ARIX Femur Nail System
K Number
K252826
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jeil Medical Corporation
Date Received
September 5, 2025
Decision Date
December 10, 2025
Product Code
HSB
Advisory Committee
Orthopedic
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
HSB Rod, Fixation, Intramedullary And Accessories

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K Number Device Name
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K242751 ARIX Pectus Bar System
K242247 ARIX Femur Nail System
K243915 FIX-C 3D Ti ACIF System
K243004 Xpine Spinal Fixation System
K231251 FlexWing Anterior Cervical Plate System
K233912 ARIX Cannulated Screw System
K231887 ARIX Ankle Distal Tibia System
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