Cleared Traditional

K200068 - Arthrex DynaNite K-Wire

K200068 is an FDA 510(k) clearance for Arthrex DynaNite K-Wire, manufactured by Arthrex, Inc.. The device is a Class 2 Orthopedic device with product code HTY cleared through the Traditional 510(k) pathway after a 168-day FDA review.

K200068 · Arthrex, Inc. · Orthopedic device
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Jun 2020
Decision
168d
Days
Class 2
Risk

K200068 is an FDA 510(k) clearance for the Arthrex DynaNite K-Wire. Classified as Pin, Fixation, Smooth (product code HTY), Class II - Special Controls.

Submitted by Arthrex, Inc. (Naples, US). The FDA issued a Cleared decision on June 29, 2020 after a review of 168 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - 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 Arthrex, Inc. devices

FDA 510(k) Submission Details - K200068

510(k) Number K200068 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 13, 2020
Decision Date June 29, 2020
Days to Decision 168 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
46d slower than avg
Panel avg: 122d · This submission: 168d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HTY Device Classification - Class 2, Special Controls

Product Code HTY Pin, Fixation, Smooth
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
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 - HTY Pin, Fixation, Smooth

All 163
Devices cleared under the same product code (HTY) and FDA review panel - the closest regulatory comparables to K200068.
VeriFixx™ Small Bone Implant
K202777 · Armis Biopharma, Inc. · Nov 2020
OSSIOfiber™ Hammertoe Fixation System/OSSIOfiber™ Hammertoe Fixation Implant
K201803 · OSSIO , Ltd. · Oct 2020
Smart Toe II, X Fuse
K201715 · Stryker GmbH · Aug 2020
OSSIOfiber™ Hammertoe Fixation System/OSSIOfiber™ Hammertoe Fixation Implant
K190652 · OSSIO , Ltd. · Mar 2020
Hammertoe Truss System (HTS)
K190926 · 4Web, Inc. · Jul 2019
Arthrex DynaNite® PIP (Hammertoe) Implant
K190287 · Arthrex, Inc. · May 2019