Vendor/Manufacturer: NuVasive
Product/Product Line: COHERE Interbody Fusion Device
Vendor/Manufacturer Catalog #: 1000-00-0716
Global Unique Device (GUD) Primary Device Identifier Number:
B14210000007160
Global Unique Device (GUD) Device Description:
COHERE Cervical cage, 14x16x7MM with 7o Lordosis
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Polymeric spinal fusion cage, sterile
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: MAX
FDA Classification Product Code Device Name:
Intervertebral Fusion Device With Bone Graft, Lumbar
Category 1: Spine
Category 2: Interbody Fusion Devices
Category 3: Cervical
Category 4: Non-Bone
SUBSTANTIALLY EQUIVALENT to the following product(s):
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