Cleared Traditional

K103015 - ODRC-DYNAMIC HIP SCREW SYSTEM

K103015 is an FDA 510(k) clearance for ODRC-DYNAMIC HIP SCREW SYSTEM, manufactured by Orthopaedic Device Research Center. The device is a Class 2 Orthopedic device with product code KTT cleared through the Traditional 510(k) pathway after a 183-day FDA review.

K103015 · Orthopaedic Device Research Center · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2011
Decision
183d
Days
Class 2
Risk

K103015 is an FDA 510(k) clearance for the ODRC-DYNAMIC HIP SCREW SYSTEM. Classified as Appliance, Fixation, Nail/blade/plate Combination, Multiple Component (product code KTT), Class II - Special Controls.

Submitted by Orthopaedic Device Research Center (Taipei, TW). The FDA issued a Cleared decision on April 13, 2011 after a review of 183 days - an extended review 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: 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 Orthopaedic Device Research Center devices

FDA 510(k) Submission Details - K103015

510(k) Number K103015 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 12, 2010
Decision Date April 13, 2011
Days to Decision 183 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
61d slower than avg
Panel avg: 122d · This submission: 183d
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 K103015.
HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM
K113327 · Stryker Corp. · Mar 2012
HOFFMANN 3 MODULAR EXTERNAL FIXATION SYSTEM
K111786 · Stryker Corp. · Jan 2012
ACE-FISCHER(R), TEMPFIX(R), HOFFMAN CLASSIC(TM) EXTERNAL FIXATORS
K112218 · DePuy Orthopaedics, Inc. · Dec 2011
SMITH & NEPHEW, INC SPATIALFRAME V4.1 WEB-BASED SOFTWARE
K110069 · Smith & Nephew, Inc. · Feb 2011
TARGON FN SYSTEM
K102057 · Aesculap Implant Systems, LLC · Dec 2010
MERETE LOCKING BONE PLATE SYSTEM II
K102688 · Merete Medical GmbH · Dec 2010