Cleared Traditional

K133967 - INTERBODY CAGE SYSTEM

K133967 is an FDA 510(k) clearance for INTERBODY CAGE SYSTEM, manufactured by Aurora Spine. The device is a Class 2 Orthopedic device with product code MAX cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K133967 · Aurora Spine · Orthopedic device
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Jan 2014
Decision
38d
Days
Class 2
Risk

K133967 is an FDA 510(k) clearance for the INTERBODY CAGE SYSTEM. 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 Aurora Spine (Washington, US). The FDA issued a Cleared decision on January 31, 2014 after a review of 38 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 Aurora Spine devices

FDA 510(k) Submission Details - K133967

510(k) Number K133967 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 24, 2013
Decision Date January 31, 2014
Days to Decision 38 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
84d faster than avg
Panel avg: 122d · This submission: 38d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MAX Device Classification - Class 2, Special Controls

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 653
Devices cleared under the same product code (MAX) and FDA review panel - the closest regulatory comparables to K133967.
CAPSTONE PTC SPINAL SYSTEM, CLYDESDALE PTC SPINAL SYSTEM
K133205 · Medtronic Sofamor Danek USA, Inc. · Mar 2014
DEROYAL SPINE SPACER SYSTEM
K131292 · Deroyal Industries, Inc. · Feb 2014
JULIET LL LATERAL LUMBAR CAGE
K133557 · Spineart · Feb 2014
ARDIS INTERBODY SYSTEM
K133184 · Zimmer Spine, Inc. · Jan 2014
MECTALIF TIPEEK
K133192 · Medacta International · Jan 2014
AESCULAP PEEK XP SPINAL IMPLANT SYSTEM
K132421 · Aesculap Implant Systems, Inc. · Jan 2014