Cleared Traditional

K170592 - NuVasive BASE Interfixated Titanium System

K170592 is an FDA 510(k) clearance for NuVasive BASE Interfixated Titanium System, manufactured by Nu Vasive, Incorporated. The device is a Class 2 Orthopedic device with product code OVD cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K170592 · Nu Vasive, Incorporated · Orthopedic device
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Apr 2017
Decision
57d
Days
Class 2
Risk

K170592 is an FDA 510(k) clearance for the NuVasive BASE Interfixated Titanium System. Classified as Intervertebral Fusion Device With Integrated Fixation, Lumbar (product code OVD), Class II - Special Controls.

Submitted by Nu Vasive, Incorporated (San Diego, US). The FDA issued a Cleared decision on April 26, 2017 after a review of 57 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

FDA 510(k) Submission Details - K170592

510(k) Number K170592 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 28, 2017
Decision Date April 26, 2017
Days to Decision 57 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
65d faster than avg
Panel avg: 122d · This submission: 57d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OVD Device Classification - Class 2, Special Controls

Product Code OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Lumbar Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft With Or Without Supplemental Fixation.
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 - OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

All 196
Devices cleared under the same product code (OVD) and FDA review panel - the closest regulatory comparables to K170592.
T-Rex Standalone ALIF
K170855 · Siats, LLC · Sep 2017
IRIX-A Lumbar Integrated Fusion System
K171567 · X-Spine Systems, Inc. · Aug 2017
Rampart One Lumbar Interbody Fusion Device
K163670 · Spineology, Inc. · May 2017
Ax Stand-Alone ALIF System
K162236 · Innovasis, Inc. · Apr 2017
Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device
K163269 · Titan Spine, LLC · Apr 2017
MectaLIF Anterior Stand Alone
K170455 · Medacta International S.A. · Mar 2017