Globus Medical, Inc.

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Web: http://www.globusmedical.com
E-Mail:
Address: 2560 General Armistead Avenue, Audubon, Pennsylvania 19403, USA
Phone: +1-(610)-415-9000 | Fax: +1-(610)-415-9144 | Map/Directions >>
 
 

Profile: Globus Medical, Inc. offers a complete suite of spinal products including fusion, MIS (minimally invasive surgery), motion preservation and biomaterials. Our portfolio includes a full line of technologically-advanced fusion products. Fusion is the primary surgical method that is used to provide pain relief from degenerative disc disease. It typically involves removing the damaged discs, restoring disc height to relieve pressure on impinged nerve roots, and fusing together adjacent vertebra to maintain the newly restored disc height. Our VIP™ (Vertical In-Line Plate) plating system is the low impact ACDF solution. The narrow width of the plate allows for a small, button-hole incision and less retraction compared to standard ACDF plating solutions. A larger diameter screw and single continuous bone interface ridge provides secure stabilization while achieving the fundamental purpose of the plate which is used to secure the bone graft. Our Providence™ is an anterior cervical plating system with a unique integrated blocking set screw that provides audible, tactile and visual confirmation of blocking mechanism engagement. In addition, the large graft windows provide visualization of graft placement and fusion status. Its integrated blocking set screw provides audible, tactile and visual confirmation. Our Assure® is an anterior cervical plating system with a unique one-step automatic blocking design. The low-profile plate is available for one to four levels in varying lengths. The plates are secured by screws that can be inserted at any angle (± 18°), available in self-tapping & self-drilling designs & rigid and variable configurations. Our products are developed, tested, evaluated & enhanced by teams of surgeons working side-by-side with engineers & machinists in the lab, in the prototype shop, and in the operating room. Our prototype shop also produces custom instrument modifications.

FDA Registration Number: 3004142400

23 Products/Services (Click for related suppliers)  
• Anterior Cervical Fusion Kit
• Anterior Cervical Plate
• Anterior Cervical Plating System
• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)
A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.
• Cervical Intervertebral Fusion Device With Bone Graft (FDA Code: ODP / 888.3080)
• Cervical Plate System
• Facet Screw Spinal Device System (FDA Code: MRW)
• Fusion Posterior Metal/Polymer Spinal System (FDA Code: NQP / 888.3070)
Pedicle screw spinal systems are multiple component devices, made from a variety of materials, including alloys such as 316L stainless steel, 316LVM stainless steel, 22Cr-13Ni-5Mn stainless steel, Ti-6Al-4V, and unalloyed titanium, that allow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. Such a spinal implant assembly consists of a combination of anchors (e.g., bolts, hooks, and/or screws); interconnection mechanisms incorporating nuts, screws, sleeves, or bolts; longitudinal members (e.g., plates, rods, and/or plate/rod combinations); and/or transverse connectors.
• Instruments for Minimally Invasive Surgery
• Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080)
• Metal Laminoplasty Plate Spine Orthosis (FDA Code: NQW / 888.3050)
A spinal interlaminal fixation orthosis is a device intended to be implanted made of an alloy, such as stainless steel, that consists of various hooks and a posteriorly placed compression or distraction rod. The device is implanted, usually across three adjacent vertebrae, to straighten and immobilize the spine to allow bone grafts to unite and fuse the vertebrae together. The device is used primarily in the treatment of scoliosis (a lateral curvature of the spine), but it also may be used in the treatment of fracture or dislocation of the spine, grades 3 and 4 of spondylolisthesis (a dislocation of the spinal column), and lower back syndrome.
• Occipito-Cervico-Thoracic Stabilization System
• Plating Systems
• Polymer Radial Hemi- Elbow Prosthesis (FDA Code: KWI / 888.3170)
An elbow joint radial (hemi-elbow) polymer prosthesis is a device intended to be implanted made of medical grade silicone elastomer used to replace the proximal end of the radius.
• Spinal Interlaminal Fixation Appliance (FDA Code: KWP / 888.3050)
• Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ / 888.3060)
A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.
• Spinal Motion Preservation System
• Spinal Pedicle Fixation Orthosis (FDA Code: MNI / 888.3070)
• Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB / 888.3070)
• Spinal Plates
• Spinal Products
• Spinal Vertebral Body Replacement Device (FDA Code: MQP / 888.3060)
• Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070)

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