Cleared Traditional

K242247 - ARIX Femur Nail System

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

K242247 · Jeil Medical Corporation · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
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

FDA 510(k) Submission Details - K242247

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.

HSB Device Classification - Class 2, Special Controls

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 460
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