Vendor/Manufacturer: Medtronic Sofamor Danek
Product/Product Line:Â ENDOSKELETON TAS NANOLOCKâ„¢
Vendor/Manufacturer Catalog #: 2320-0112-N
Global Unique Device (GUD) Primary Device Identifier Number:Â
00191375018452
Global Unique Device (GUD) Device Description:Â
Interbody Fusion Device 6 Degree Medium 6mm
Category 1: Spine
Category 2: Interbody Fusion Devices
Category 3:Â Lumbar/T-Lumbar
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Metallic spinal interbody fusion cage
Global Medical Device Nomenclature (GMDN) Definition:
A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
FDA Regulation Medical Specialty:Â
Orthopedic Devices - Prosthetic Devices
FDA Regulation Number:Â 888.3080
FDA Regulation Description Classification Name:Â
Intervertebral body fusion device
FDA Classification Product Code:Â OVD
FDA Classification Product Code Device Name:Â
Intervertebral fusion device with integrated fixation, lumbar
The Medtronic Sofamor Danek ENDOSKELETON TAS NANOLOCKâ„¢
Interbody Fusion Devices are SUBSTANTIALLY EQUIVALENT to the following product(s):
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