Cleared Traditional

K091258 - EXTRAFIX EXTERNAL FIXATION SYSTEM

K091258 is an FDA 510(k) clearance for EXTRAFIX EXTERNAL FIXATION SYSTEM, manufactured by Qfx Technologies, Inc.. The device is a Class 2 Orthopedic device with product code KTT cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K091258 · Qfx Technologies, Inc. · Orthopedic device
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Optimized for regulatory review, auditing and printing
Jul 2009
Decision
86d
Days
Class 2
Risk

K091258 is an FDA 510(k) clearance for the EXTRAFIX EXTERNAL FIXATION SYSTEM. Classified as Appliance, Fixation, Nail/blade/plate Combination, Multiple Component (product code KTT), Class II - Special Controls.

Submitted by Qfx Technologies, Inc. (Alexandria, US). The FDA issued a Cleared decision on July 24, 2009 after a review of 86 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 Qfx Technologies, Inc. devices

FDA 510(k) Submission Details - K091258

510(k) Number K091258 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 29, 2009
Decision Date July 24, 2009
Days to Decision 86 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d faster than avg
Panel avg: 122d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KTT Device Classification - Class 2, Special Controls

Product Code KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
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 - KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

All 316
Devices cleared under the same product code (KTT) and FDA review panel - the closest regulatory comparables to K091258.
AFGHAN EXTERNAL FIXATOR
K092002 · Smith & Nephew, Inc. · Dec 2009
BIOMET VISION FOOTRING SYSTEM
K093057 · Ebi, L.P. · Dec 2009
HOFFMAN XPRESS LINE EXTENSION
K092834 · Howmedica Osteonics Corp. · Oct 2009
SMITH & NEPHEW RAIL SYSTEM
K090926 · Smith & Nephew, Inc. · Jun 2009
ACE FISCHER EXTERNAL FIXATION SYSTEM
K083789 · DePuy Orthopaedics, Inc. · Mar 2009
REPROCESSED EXTERNAL FIXATION DEVICE
K083636 · Sterilmed, Inc. · Mar 2009