Vendor/Manufacturer: LifeNet
Product/Product Line: VERTIGRAFT 1 Interbody Fusion Device
Vendor/Manufacturer Catalog #: VG1B-14HAP
Global Unique Device (GUD) Primary Device Identifier Number:
NA
Global Unique Device (GUD) Device Description:
NA
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
NA
FDA Regulation Medical Specialty:
NA
FDA Regulation Number: NA
FDA Regulation Description Classification Name:
NA
FDA Classification Product Code: NA
FDA Classification Product Code Device Name:
NA
Category 1: Spine
Category 2: Interbody Fusion Devices
Category 3: Lumbar
Category 4: Bone
FDA Premarket Submissions: NA
SUBSTANTIALLY EQUIVALENT to the following product(s):
1. NA
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