Cleared Traditional

K192592 - Axis Plating System

K192592 is the FDA 510(k) clearance for Axis Plating System by Extremity Medical, LLC. It is a Class 2 Orthopedic device (product code HRS) cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K192592 · Extremity Medical, LLC · Orthopedic device
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Nov 2019
Decision
62d
Days
Class 2
Risk

K192592 is an FDA 510(k) clearance for the Axis Plating System. Classified as Plate, Fixation, Bone within the HRS classification (a category comprising bone fixation plates and orthopedic hardware), Class II - Special Controls.

Submitted by Extremity Medical, LLC (Parsippany, US). The FDA issued a Cleared decision on November 21, 2019 after a review of 62 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Extremity Medical, LLC devices

Submission Details

510(k) Number K192592 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 20, 2019
Decision Date November 21, 2019
Days to Decision 62 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
60d faster than avg
Panel avg: 122d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HRS Plate, Fixation, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
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 - HRS Plate, Fixation, Bone

All 914
Devices cleared under the same product code (HRS) and FDA review panel - the closest regulatory comparables to K192592.
Nebula Brand Locking Bone Plates and Screws Osteosynthesis Plating System, Nebula Brand of DHS Plating System
K191793 · Nebula Surgical Private Limited · Dec 2019
Exsomed Wrist Plating System
K192473 · Exsomed Corporation · Dec 2019
VariAx Foot
K192675 · Stryker GmbH · Nov 2019
PolyLock Small Bone Plating System
K192323 · Fusion Orthopedics, LLC · Nov 2019
TDM Plate and Screw Systems
K190391 · Tdm Co., Ltd. · Nov 2019
ARIX Wrist System
K191972 · Jeil Medical Corporation · Nov 2019