Cleared Traditional

K060118 - SSP PEDICLE SCREW SYSTEM

K060118 is an FDA 510(k) clearance for SSP PEDICLE SCREW SYSTEM, manufactured by Specialty Spine Products, LLC. The device is a Class 2 Orthopedic device with product code MNH cleared through the Traditional 510(k) pathway after a 142-day FDA review.

K060118 · Specialty Spine Products, LLC · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2006
Decision
142d
Days
Class 2
Risk

K060118 is an FDA 510(k) clearance for the SSP PEDICLE SCREW SYSTEM. Classified as Orthosis, Spondylolisthesis Spinal Fixation (product code MNH), Class II - Special Controls.

Submitted by Specialty Spine Products, LLC (San Diego, US). The FDA issued a Cleared decision on June 8, 2006 after a review of 142 days - within the typical 510(k) review window.

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 Specialty Spine Products, LLC devices

FDA 510(k) Submission Details - K060118

510(k) Number K060118 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 17, 2006
Decision Date June 08, 2006
Days to Decision 142 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
20d slower than avg
Panel avg: 122d · This submission: 142d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNH Device Classification - Class 2, Special Controls

Product Code MNH Orthosis, Spondylolisthesis Spinal 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 - MNH Orthosis, Spondylolisthesis Spinal Fixation

All 208
Devices cleared under the same product code (MNH) and FDA review panel - the closest regulatory comparables to K060118.
NUVASIVE SPHERX II SYSTEM
K061778 · Nuvasive, Inc. · Jul 2006
ZODIAC ADJUSTABLE BRIDGES, MODELS 11-20XX,11-25XX,11-30XX,11-35XX
K061321 · Alphatec Spine, Inc. · Jul 2006
4CIS VANE SPINE SYSTEM
K060702 · Solco Biomedical Co., Ltd. · Jun 2006
NUVASIVE SPHERX SYSTEM
K060225 · Nuvasive, Inc. · Apr 2006
GSS PEDICLE SCREW SYSTEM
K053573 · GS Medical Co., Ltd. · Mar 2006
XIA 4.5 SPINAL SYSTEM
K050461 · Stryker Spine · Jul 2005