Cleared Traditional

K180755 - Vail ALIF Buttress Plate System

K180755 is the FDA 510(k) clearance for Vail ALIF Buttress Plate System by Evolution Spine, LLC. It is a Class 2 Orthopedic device (product code KWQ) cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K180755 · Evolution Spine, LLC · Orthopedic device
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Jul 2018
Decision
106d
Days
Class 2
Risk

K180755 is an FDA 510(k) clearance for the Vail ALIF Buttress Plate System. Classified as Appliance, Fixation, Spinal Intervertebral Body (product code KWQ), Class II - Special Controls.

Submitted by Evolution Spine, LLC (Dallas, US). The FDA issued a Cleared decision on July 6, 2018 after a review of 106 days - within the typical 510(k) review window.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3060 - 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 Evolution Spine, LLC devices

Submission Details

510(k) Number K180755 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 22, 2018
Decision Date July 06, 2018
Days to Decision 106 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
16d faster than avg
Panel avg: 122d · This submission: 106d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KWQ Appliance, Fixation, Spinal Intervertebral Body
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3060
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 - KWQ Appliance, Fixation, Spinal Intervertebral Body

All 421
Devices cleared under the same product code (KWQ) and FDA review panel - the closest regulatory comparables to K180755.
Athena Cervical Plate System
K180022 · Medyssey USA, Inc. · Jul 2018
Kestrel™ Buttress Plate System
K181063 · Innovasis, Inc. · Jul 2018
Zavation Cervical Plate System
K181244 · Zavation Medical Products, LLC · Jul 2018
Life Spine Lumbar Fixation System (SENTRY)
K180166 · Life Spine, Inc. · Jun 2018
Cure™ Lumbar Plate System
K180090 · Meditech Spine, LLC · Apr 2018
Mediant Anterior Cervical Plating System
K173935 · Intelligent Implant Systems, LLC · Apr 2018