Cleared Traditional

K201820 - NuVasive Thoracolumbar Interbody System...

K201820 is the FDA 510(k) clearance for NuVasive Thoracolumbar Interbody System... by Nu Vasive, Incorporated. It is a Class 2 Orthopedic device (product code MAX) cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K201820 · Nu Vasive, Incorporated · Orthopedic device
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Sep 2020
Decision
86d
Days
Class 2
Risk

K201820 is an FDA 510(k) clearance for the NuVasive Thoracolumbar Interbody Systems: CoRoent Thoracolumbar System, CoRoe.... Classified as Intervertebral Fusion Device With Bone Graft, Lumbar within the MAX classification (a category for intervertebral fusion devices and spinal implants), Class II - Special Controls.

Submitted by Nu Vasive, Incorporated (San Diego, US). The FDA issued a Cleared decision on September 25, 2020 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3080 - 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 Nu Vasive, Incorporated devices

Submission Details

510(k) Number K201820 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 2020
Decision Date September 25, 2020
Days to Decision 86 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
36d faster than avg
Panel avg: 122d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft.
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 - MAX Intervertebral Fusion Device With Bone Graft, Lumbar

All 603
Devices cleared under the same product code (MAX) and FDA review panel - the closest regulatory comparables to K201820.
GAIA Lumbar Interbody Fusion Device (LIFD) Family
K201939 · Printerprezz · Oct 2020
Fortilink Cages with TiPlus Technology
K201453 · Paradigm Spine GmbH · Oct 2020
NuVasive® Cohere® Thoracolumbar Interbody System
K200953 · Nu Vasive, Incorporated · Oct 2020
FlareHawk TiHawk9 Interbody Fusion System
K201367 · Integrity Implants, Inc. · Sep 2020
X-Pac Expandable Lumbar Cage System
K201145 · Expanding Innovations, Inc. · Sep 2020
TruLift Expandable Spacer System
K201721 · Life Spine, Inc. · Sep 2020