Cleared Traditional

K172620 - SyndesMetrics Syndesmosis Repair System

K172620 is an FDA 510(k) clearance for SyndesMetrics Syndesmosis Repair System, manufactured by Mortise Medical, LLC. The device is a Class 2 Orthopedic device with product code HTN cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K172620 · Mortise Medical, LLC · Orthopedic device
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Nov 2017
Decision
69d
Days
Class 2
Risk

K172620 is an FDA 510(k) clearance for the SyndesMetrics Syndesmosis Repair System. Classified as Washer, Bolt Nut (product code HTN), Class II - Special Controls.

Submitted by Mortise Medical, LLC (Logan, US). The FDA issued a Cleared decision on November 8, 2017 after a review of 69 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 Mortise Medical, LLC devices

FDA 510(k) Submission Details - K172620

510(k) Number K172620 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 2017
Decision Date November 08, 2017
Days to Decision 69 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
53d faster than avg
Panel avg: 122d · This submission: 69d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HTN Device Classification - Class 2, Special Controls

Product Code HTN Washer, Bolt Nut
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 - HTN Washer, Bolt Nut

All 86
Devices cleared under the same product code (HTN) and FDA review panel - the closest regulatory comparables to K172620.
Infinity-Lock Button System
K180243 · Xiros, Ltd. · Apr 2018
PUMA System
K171703 · Panther Orthopedics, Inc. · Mar 2018
Akros FibuLink™ Syndesmosis Repair Kit
K173550 · Akros Medical · Dec 2017
GRAVITY™ Syndesmosis LP
K170249 · Wrightmedicaltechnologyinc · Jun 2017
INVISIKNOT Ankle Syndesmosis Repair Kit
K162996 · Smith & Nephew, Inc. · Jun 2017
KISSloc Suture System
K170440 · Arthrosurface, Inc. · May 2017