Cleared Traditional

K190227 - Boomerang Anterior Cervical Plate System

K190227 is the FDA 510(k) clearance for Boomerang Anterior Cervical Plate System by Choicespine, LP. It is a Class 2 Orthopedic device (product code KWQ) cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K190227 · Choicespine, LP · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2019
Decision
85d
Days
Class 2
Risk

K190227 is an FDA 510(k) clearance for the Boomerang™ Anterior Cervical Plate System. Classified as Appliance, Fixation, Spinal Intervertebral Body (product code KWQ), Class II - Special Controls.

Submitted by Choicespine, LP (Knoxville, US). The FDA issued a Cleared decision on May 1, 2019 after a review of 85 days - a notably fast clearance cycle.

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: 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 Choicespine, LP devices

Submission Details

510(k) Number K190227 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 2019
Decision Date May 01, 2019
Days to Decision 85 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
37d faster than avg
Panel avg: 122d · This submission: 85d
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 373
Devices cleared under the same product code (KWQ) and FDA review panel - the closest regulatory comparables to K190227.
CAYMAN LP Plate System
K190584 · K2m, Inc. · May 2019
MVP Cervical Plate System
K190170 · GS Medical Co., Ltd. · May 2019
CYGNUS™ Anterior Cervical Plate System
K190666 · MiRus, LLC · May 2019
ASSURE® Anterior Cervical Plate System
K183056 · Globus Medical, Inc. · Apr 2019
CastleLoc-P Anterior Cervical Plate System
K190425 · L & K Biomed Co., Ltd. · Mar 2019
SMG Anterior Cervical Plate System
K183073 · Sapphire Medical Group · Feb 2019