Cleared Traditional

K143490 - VERTA Corpectomy Cage

K143490 is an FDA 510(k) clearance for VERTA Corpectomy Cage, manufactured by Camber Spine. The device is a Class 2 Orthopedic device with product code MQP cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K143490 · Camber Spine · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2015
Decision
49d
Days
Class 2
Risk

K143490 is an FDA 510(k) clearance for the VERTA Corpectomy Cage. Classified as Spinal Vertebral Body Replacement Device (product code MQP), Class II - Special Controls.

Submitted by Camber Spine (Wayne, US). The FDA issued a Cleared decision on January 26, 2015 after a review of 49 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 Camber Spine devices

FDA 510(k) Submission Details - K143490

510(k) Number K143490 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 2014
Decision Date January 26, 2015
Days to Decision 49 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
73d faster than avg
Panel avg: 122d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQP Device Classification - Class 2, Special Controls

Product Code MQP Spinal Vertebral Body Replacement Device
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 - MQP Spinal Vertebral Body Replacement Device

All 201
Devices cleared under the same product code (MQP) and FDA review panel - the closest regulatory comparables to K143490.
NuVasive PEEK Corpectomy System
K151167 · Nu Vasive, Incorporated · Sep 2015
NuVasive X-CORE(R) Expandable VBR System
K142205 · Nuvasive, Inc. · Feb 2015
StaXx(R) XD System
K142996 · Spine Wave, Inc. · Feb 2015
CAPRI
K142016 · K2m, Inc. · Nov 2014
AIS MODULIFT VBR SYSTEM
K142150 · Aesculap Implant System, Inc. · Oct 2014
LATERAL VBR SYSTEM
K140563 · Nu Vasive, Incorporated · Aug 2014