NuVasive COHERE. Interbody Fusion Device. Cervical. Non-Bone. Catalog #1000-00-0716

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

FDA Premarket Submissions: K200953 , K201820

SUBSTANTIALLY EQUIVALENT to the following product(s):

Recent Posts