Cleared Traditional

K242247 - ARIX Femur Nail System

K242247 is the FDA 510(k) clearance for ARIX Femur Nail System by Jeil Medical Corporation. It is a Class 2 Orthopedic device (product code HSB) cleared through the Traditional 510(k) pathway after a 265-day FDA review.

K242247 · Jeil Medical Corporation · Orthopedic device
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Apr 2025
Decision
265d
Days
Class 2
Risk

K242247 is an FDA 510(k) clearance for the ARIX Femur Nail System. Classified as Rod, Fixation, Intramedullary And Accessories (product code HSB), Class II - Special Controls.

Submitted by Jeil Medical Corporation (Seoul, KR). The FDA issued a Cleared decision on April 22, 2025 after a review of 265 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3020 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Jeil Medical Corporation devices

Submission Details

510(k) Number K242247 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 31, 2024
Decision Date April 22, 2025
Days to Decision 265 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
143d slower than avg
Panel avg: 122d · This submission: 265d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HSB Rod, Fixation, Intramedullary And Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3020
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - HSB Rod, Fixation, Intramedullary And Accessories

All 318
Devices cleared under the same product code (HSB) and FDA review panel - the closest regulatory comparables to K242247.
Succession™ AFN System
K250622 · Ortho Solutions UK , Ltd. · Aug 2025
Phantom® Hindfoot TTC/TC Nail System
K251850 · Paragon 28, Inc. · Jul 2025
GMReis Fibula Nail System
K250559 · Gm Dos Reis Industria E Comercio · Jun 2025
FitboneTM Trochanteric
K250112 · Orthofix Srl · Apr 2025
Pediatric Nailing Platform Tibia Pediatric Nailing Platform Femur
K250623 · OrthoPediatrics Corp. · Apr 2025
Fassier-Duval Telescoping IM System
K241983 · Orthopediatrics Canada Ulc Dba Pega Medical · Feb 2025