Vendor/Manufacturer: Nuvasive
Product/Product Line: ARCHON Plate
Vendor/Manufacturer Catalog #: 8787238
Global Unique Device (GUD) Primary Device Identifier Number: 00887517209313
Global Unique Device (GUD) Device Description:
Archon Plate, 38mm 2-Level
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Spinal fixation plate, non-bioabsorbable
Category 1: Spine
Category 2: Cervical Plate & Screw Systems
Category 3: Plate
Category 4: Two Level
Quantity of "Each"es needed in each System/Set: 1
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
SUBSTANTIALLY EQUIVALENT to the following products:
Opmerkingen