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Precision Spine AccuFit® Lateral Plate System. Catalog #58-VS-6560

  • Writer: CataBlog
    CataBlog
  • May 22, 2022
  • 1 min read

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Vendor/Manufacturer: Precision Spine

Product/Product Line: AccuFit® Lateral Plate System

Vendor/Manufacturer Catalog #: 58-VS-6560

Global Unique Device (GUD) Primary Device Identifier Number: 00840019904636

Global Unique Device (GUD) Device Description:

Ø6.5mm Variable Screw, 60mm

Global Medical Device Nomenclature (GMDN) Preferred Term Name:

Spinal bone screw, non-bioabsorbable

Global Medical Device Nomenclature (GMDN) Definition:

A small, threaded rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a stabilization device (e.g., rod, plate) to bone; it 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 available in various types, including pedicle and transfacet, and is typically used to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities.


Category 1: Spine

Category 2: Thoracolumbar Plate & Screw Systems

Category 3: Screw


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: K162211


The Precision Spine AccuFit® Lateral Plate System is

SUBSTANTIALLY EQUIVALENT to the following products:



For more information, please visit us at Infonomics.com

 
 
 

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