Vendor/Manufacturer: Amedica
Product/Product Line: TAURUS Lumbar Pedicle Screw System
Vendor/Manufacturer Catalog #: 25-2000-040
Global Unique Device (GUD) Primary Device Identifier Number:
M555252000040
Global Unique Device (GUD) Device Description:
Taurus Pedicle Screw System-Curved Rod 5.5x40mm
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Bone-screw internal spinal fixation system, non-sterile
Category 1: Spine
Category 2: Lumbar Pedicle Screw Systems
Category 3: Rod
Category 4: One Level
Quantity of "Each"es needed in each System/Set: 2
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
SUBSTANTIALLY EQUIVALENT to the following products:
1. NA
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