Vendor/Manufacturer: DePuy Synthes
Product/Product Line: EXPEDIUM VERSE® Spine System
Vendor/Manufacturer Catalog #: 199721640
Global Unique Device (GUD) Primary Device Identifier Number: 10705034442280
Global Unique Device (GUD) Device Description:
EXPEDIUM VERSE SPINE SYSTEM POLYAXIAL SCREW 5.5 6.0 x 40mm
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Bone-screw internal spinal fixation system, non-sterile
Global Medical Device Nomenclature (GMDN) Definition:
An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.
FDA Regulation Medical Specialty:
Orthopedic Devices - Prosthetic Devices
FDA Regulation Number: 888.3070
FDA Regulation Description Classification Name:
Thoracolumbosacral pedicle screw system
FDA Classification Product Code(s): KWP, KWQ, MNH, MNI, NKB, OSH
FDA Classification Product Code Device Name(s):
KWP: Appliance, Fixation, Spinal Interlaminal
KWQ: Appliance, Fixation, Spinal Intervertebral Body
MNH: Orthosis, spondylolisthesis spinal fixation
MNI: Orthosis, Spinal Pedicle Fixation
NKB: Thoracolumbosacral Pedicle Screw System
OSH: Pedicle screw spinal system, adolescent idiopathic scoliosis
The DePuy Synthes EXPEDIUM VERSE® Spine System is SUBSTANTIALLY EQUIVALENT to the following product(s):
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