Nuvasive Inc.

Address: 4545, Towne Centre Court, San Diego, California 92121, USA
Phone: +1-(800)-455-1476 | Fax: +1-(858)-909-2000 | Map/Directions >>

Profile: Nuvasive Inc. focuses on the design, development and marketing of products for the surgical treatment of spinal disorders. We provide safe & reproductive procedural solutions with platform technology for treatment of lumbar and cervical degenerative conditions. Our proprietary maximum access surgery technology renders significant benefits to surgeons & patients including reduced surgery time, shorter hospital stay and faster recovery times.

The company was founded in 1997. NASDAQ:NUVA (SEC Filings)

FDA Registration Number: 2031966

36 Products/Services (Click for related suppliers)  
• AC-Powered Nerve Stimulator (FDA Code: BXM / 868.2775)
An electrical peripheral nerve stimulator (neuromuscular blockade monitor) is a device used to apply an electrical current to a patient to test the level of pharmacological effect of anesthetic drugs and gases.
• Arthroscopes (FDA Code: HRX / 888.1100)
An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.
• Arthroscopic Accessories (FDA Code: NBH / 888.1100)
• Bilateral Facet Screws
• Bipolar Electrode Cables
• 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.
• Cement Restrictor Hip Prosthesis (FDA Code: JDK / 878.3300)
Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.
• Cutaneous Electrode (FDA Code: GXY / 882.1320)
A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.
• Detachable Needle Electrode Cables & Accessories
• Diagnostic Electromyograph (FDA Code: IKN / 890.1375)
A diagnostic electromyograph is a device intended for medical purposes, such as to monitor and display the bioelectric signals produced by muscles, to stimulate peripheral nerves, and to monitor and display the electrical activity produced by nerves, for the diagnosis and prognosis of neuromuscular disease.
• Electrode Cables (FDA Code: IKD / 890.1175)
An electrode cable is a device composed of strands of insulated electrical conductors laid together around a central core and intended for medical purposes to connect an electrode from a patient to a diagnostic machine.
• Electrosurgical Electrode Cables
• ENT Nerve Stimulator (FDA Code: ETN / 874.1820)
A surgical nerve stimulator/locator is a device that is intended to provide electrical stimulation to the body to locate and identify nerves and to test their excitability.
• Evaluated Facet Screws
• Evoked Response Electrical Stimulator (FDA Code: GWF / 882.1870)
An evoked response electrical stimulator is a device used to apply an electrical stimulus to a patient by means of skin electrodes for the purpose of measuring the evoked response.
• Facet Screw Spinal Device System (FDA Code: MRW)
• Facet Screws
• Fiberoptic Surgical Light (FDA Code: FST / 878.4580)
A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.
• Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080)
• Metal Mesh (FDA Code: EZX / 878.3300)
• Monopolar Electrode Cables
• Neurological Stereotaxic Instrument (FDA Code: HAW / 882.4560)
A stereotaxic instrument is a device consisting of a rigid frame with a calibrated guide mechanism for precisely positioning probes or other devices within a patient's brain, spinal cord, or other part of the nervous system.
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.
• Polymeric Surgical Mesh (FDA Code: FTL / 878.3300)
• Posterior Cervical Plating Systems
• Powered Wheeled Stretcher (FDA Code: INK / 890.3690)
A powered wheeled stretcher is a battery-powered table with wheels that is intended for medical purposes for use by patients who are unable to propel themselves independently and who must maintain a prone or supine position for prolonged periods because of skin ulcers or contractures (muscle contractions).
• Spinal Interlaminal Fixation Appliance (FDA Code: KWP / 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.
• 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 Pedicle Fixation Orthosis (FDA Code: MNI / 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.
• Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB / 888.3070)
• Spinal Vertebral Body Replacement Device (FDA Code: MQP / 888.3060)
• Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070)
• Surgical Mesh (FDA Code: FTM / 878.3300)
• Transarticular Facet Screws
• Translaminar Facet Screws
• Tripolar Electrode Cables

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