Vendor/Manufacturer: Nuvasive
Product/Product Line: BASE ALIF
Vendor/Manufacturer Catalog #: 6952815
Global Unique Device (GUD) Primary Device Identifier Number: 00887517701091
Global Unique Device (GUD) Device Description:
BASE Ti Implant, 8x38x28mm 15°
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Metallic spinal fusion cage, non-sterile
Category 1: Spine
Category 2: Interbody Fusion with Integrated Screws - Lumbar/T-Lumbar
Category 3: ALIF
Category 4: Lumbar/T-Lumbar
Quantity of "Each"es needed in each System/Set: 1
FDA Regulation Medical Specialty:
Orthopedic Devices - Prosthetic Devices
FDA Regulation Number: 888.3080
FDA Regulation Description Classification Name:
Intervertebral body fusion device
FDA Classification Product Code: OVD
FDA Classification Product Code Device Name:
Intervertebral Fusion Device With Integrated Fixation, Lumbar
SUBSTANTIALLY EQUIVALENT to the following products:
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