Cleared Special

K140696 - STREAMLINE TL SPINAL FIXATION SYSTEM

K140696 is an FDA 510(k) clearance for STREAMLINE TL SPINAL FIXATION SYSTEM, manufactured by Pioneer Surgical Technology, Inc.. The device is a Class 2 Orthopedic device with product code NKB cleared through the Special 510(k) pathway after a 22-day FDA review.

K140696 · Pioneer Surgical Technology, Inc. · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2014
Decision
22d
Days
Class 2
Risk

K140696 is an FDA 510(k) clearance for the STREAMLINE TL SPINAL FIXATION SYSTEM. Classified as Thoracolumbosacral Pedicle Screw System within the NKB classification (a category for thoracolumbosacral pedicle screw systems), Class II - Special Controls.

Submitted by Pioneer Surgical Technology, Inc. (Marquette, US). The FDA issued a Cleared decision on April 10, 2014 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3070 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Pioneer Surgical Technology, Inc. devices

FDA 510(k) Submission Details - K140696

510(k) Number K140696 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 2014
Decision Date April 10, 2014
Days to Decision 22 days
Submission Type Special
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
100d faster than avg
Panel avg: 122d · This submission: 22d
Pathway characteristics
Modification to existing cleared device.

NKB Device Classification - Class 2, Special Controls

Product Code NKB Thoracolumbosacral Pedicle Screw System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3070
Definition Intended To Provide Immobilization And Stabilization Of Spinal Segments In Thoracic, Lumbar, And Sacral Spine As An Adjunct To Fusion.
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 - NKB Thoracolumbosacral Pedicle Screw System

All 874
Devices cleared under the same product code (NKB) and FDA review panel - the closest regulatory comparables to K140696.
POLARIS SPINAL SYSTEM -TRANSLATION SCREW
K140123 · Ebi, LLC · Apr 2014
FORTRESS PEDICLE SCREW SYSTEM
K140010 · Spineology, Inc. · Apr 2014
PICASSO II MIS SPINAL SYSTEM
K140219 · Accel Spine · Apr 2014
ORTHROS POSTERIOR STABILIZATION SYSTEM
K133366 · Camber Spine · Apr 2014
BAXANO SURGICAL MIS SPINAL SYSTEM
K133743 · Baxano Surgical, Inc. · Apr 2014
CD HORIZON SPINAL SYSTEM
K140449 · Medtronic Sofamor Danek, Inc. · Mar 2014