Cleared Traditional

K033826 - ORTHOPEDIC ALLIANCE SPINE SYSTEM

K033826 is an FDA 510(k) clearance for ORTHOPEDIC ALLIANCE SPINE SYSTEM, manufactured by Orthopedic Alliance, LLC. The device is a Class 2 Orthopedic device with product code MNI cleared through the Traditional 510(k) pathway after a 204-day FDA review.

K033826 · Orthopedic Alliance, LLC · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2004
Decision
204d
Days
Class 2
Risk

K033826 is an FDA 510(k) clearance for the ORTHOPEDIC ALLIANCE SPINE SYSTEM. Classified as Orthosis, Spinal Pedicle Fixation (product code MNI), Class II - Special Controls.

Submitted by Orthopedic Alliance, LLC (Murrieta, US). The FDA issued a Cleared decision on July 1, 2004 after a review of 204 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3070 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Orthopedic Alliance, LLC devices

FDA 510(k) Submission Details - K033826

510(k) Number K033826 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 2003
Decision Date July 01, 2004
Days to Decision 204 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
82d slower than avg
Panel avg: 122d · This submission: 204d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNI Device Classification - Class 2, Special Controls

Product Code MNI Orthosis, Spinal Pedicle Fixation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3070
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 - MNI Orthosis, Spinal Pedicle Fixation

All 216
Devices cleared under the same product code (MNI) and FDA review panel - the closest regulatory comparables to K033826.
MODIFICATION TO BLACKSTONE MODULAR PEDICLE SCREW SYSTEM
K042514 · Blackstone Medical, Inc. · Oct 2004
BLACKSTONE ASCENT POCT SYSTEM 5.5MM/3.0MM SINGLE AXIAL CONNECTOR
K042100 · Blackstone Medical, Inc. · Sep 2004
MODIFICATION TO CD HORIZON SPINAL SYSTEM
K041777 · Medtronic Sofamor Danek · Sep 2004
MODIFICATION TO CD HORIZON SPINAL SYSTEM
K041030 · Medtronic Sofamor Danek · Jun 2004
SUMMIT OCT SPINAL SYSTEM
K041203 · Depuy Spine, Inc. · Jun 2004
MODIFICATION TO CD HORIZON SPINAL SYSTEM
K041118 · Medtronic Sofamor Danek · May 2004