Vendor/Manufacturer: Stryker
Product/Product Line: LITe® Plate System
Vendor/Manufacturer Catalog #: 49175022
Global Unique Device (GUD) Primary Device Identifier Number: 07613327068078
Global Unique Device (GUD) Device Description:
Standard Screw
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Spinal fixation plate, non-bioabsorbable
Global Medical Device Nomenclature (GMDN) Definition:
A small implantable sheet of solid material that is attached to the spine with screws for spinal immobilization and is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). The device is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities (e.g., during anterior/posterior cervical, anterior/posterior lumbar, thoracolumbar, and occipital fixation procedures).
FDA Regulation Medical Specialty: Orthopedic Devices - Prosthetic Devices
FDA Regulation Number: 888.3060
FDA Regulation Description Classification Name:
Spinal intervertebral body fixation orthosis
FDA Classification Product Code: KWQ
FDA Classification Product Code Device Name:
Appliance, Fixation, Spinal Intervertebral Body
FDA Premarket Submission: K150449
The Stryker LITe® Plate System is
SUBSTANTIALLY EQUIVALENT to the following product:
For more information, please visit us at Infonomics.com
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