Cleared Traditional

K112025 - SURE LOK MINI POSTERIOR CERVICAL/UPPER ...

K112025 is an FDA 510(k) clearance for SURE LOK MINI POSTERIOR CERVICAL/UPPER ..., manufactured by Spinal USA. The device is a Class 2 Orthopedic device with product code KWP cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K112025 · Spinal USA · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2011
Decision
62d
Days
Class 2
Risk

K112025 is an FDA 510(k) clearance for the SURE LOK MINI POSTERIOR CERVICAL/UPPER THORACIC SYSTEM. Classified as Appliance, Fixation, Spinal Interlaminal (product code KWP), Class II - Special Controls.

Submitted by Spinal USA (Pear, US). The FDA issued a Cleared decision on September 15, 2011 after a review of 62 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3050 - 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 Spinal USA devices

FDA 510(k) Submission Details - K112025

510(k) Number K112025 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 15, 2011
Decision Date September 15, 2011
Days to Decision 62 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
60d faster than avg
Panel avg: 122d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KWP Device Classification - Class 2, Special Controls

Product Code KWP Appliance, Fixation, Spinal Interlaminal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3050
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 - KWP Appliance, Fixation, Spinal Interlaminal

All 309
Devices cleared under the same product code (KWP) and FDA review panel - the closest regulatory comparables to K112025.
OASYS SPINAL SYSTEM
K111719 · Stryker Spine · Jan 2012
CASPIAN
K113654 · K2m, Inc. · Jan 2012
AXLE PEEK INTERSPINOUS FUSION SYSTEM
K112592 · X-Spine Systems, Inc. · Dec 2011
BRIDGEPOINT SPINOUS PROCESS CAMP- POSTERIOR FIXATION SYSTEM
K103205 · Alphatec Spine, Inc. · Jun 2011
ASCENT POSTERIOR OCCIPITAL THORACIC (POCT) SYSTEM (TITANIUM & COBALT CHROME RODS)
K111183 · Orthofix, Inc. · May 2011
ELLIPSE OCCIPITO-CERVICO-THORACIC SPINAL SYSTEM
K110963 · Globus Medical, Inc. · May 2011