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NuVasive Inc.

NuVasive Launches Pulse™

The company reports Pulse is engineered to improve workflow, reduce variability and increase surgical reproducibility, Pulse addresses a broader range of clinical challenges in the operating room (OR) compared to any other enabling technology in the spine market.

NuVasive Announces Commercial Launch of Modulus® TLIF-O

Modulus® TLIF-O features porous surface technology that, based on pre-clinical data, provides a favorable environment for bone in-growth and bone on-growth, and consistently achieves stronger osseointegration than solid implants with smooth or rough surfaces.

NuVasive Grows Cervical Spinal Interbody Portfolio With PEEK Corpectomy Implant

12/10/18: Received 510(k) clearance from the FDA for expanded use of its Monolith® Corpectomy System, providing surgeons with a modular PEEK interbody solution for cervical corpectomy procedures.

NuVasive Launches TLX® 20 Degree Expandable Spinal Interbody Implant

9/5/18: "The TLX 20 system is an innovative device that can improve surgical workflow and patient outcomes by easily and actively enhancing the segmental alignment and interspace height," said Dr. Christopher Shaffrey, neurosurgeon at University of Virginia Health System.

First Porous PEEK Spinal Implant Clinical Study Validates NuVasive Advanced Materials Science Technology In Treating Degenerative Cervical Disc Disease

6/20/18: "This interbody fusion device with Porous PEEK surface technology provided improved osseointegration and supported spinal fusion in single level and multi-level cervical fusions," said Dr. J. Kenneth Burkus of the Hughston Clinic in Columbus, Ga. "Twelve-month clinical outcomes have demonstrated the efficacy and stability of the Cohere Porous PEEK interbody device and shown that it is a clinically viable implant alternative for achieving successful clinical and radiological outcomes in cervical spine fusion surgery, particularly in multi-level or revision surgeries where fusion rates are lower."

NuVasive PRECICE STRYDE™ System Used In First Patient For Stature Lengthening By International Limb Lengthening Expert

5/22/18: "The PRECICE STRYDE technology advances how I am able to treat patients requiring limb reconstruction or those seeking to increase their height, and I am excited to incorporate this into my practice," said Dr. Paley, a board-certified orthopedic surgeon specializing in limb lengthening and deformity correction. "I continually seek to offer better clinical solutions to my patients, and I am proud to have collaborated with NuVasive in the development of this latest orthopedic advancement."

NuVasive Extends Its Leadership As Lateral Spine Technology Innovator With New Lateral Single-Position Surgery Procedure

HOME NuVasive, Inc. (NASDAQ: NUVA), the leader in spine technology innovation, focused on transforming spine surgery with minimally disruptive, procedurally-integrated solutions, today...

NuVasive Receives Expanded FDA 510(k) Clearance For Innovative Magnetic Limb Lengthening Technology

HOME New Additional Clearance for the Company's PRECICE® system includes fracture fixation, pseudoarthrosis, malunions, nonunions and bone transport NuVasive, Inc. (NASDAQ: NUVA),...

NuVasive, Medtronic Lead U.S. Minimally Invasive Spinal Implant Market Due to Increased Target Population Requiring Surgical Procedures

According to a new series of reports on the U.S. minimally invasive spinal (MIS) implants market by iData Research (www.idataresearch.com), growth has increased across...

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New Study Validates Rigorous Safety Measures Needed To Reduce Mercury Exposure During Dental Amalgam Filling Removal

"For decades, our non-profit organization has been concerned about this issue and collected research about amalgam fillings, all of which contain approximately 50% mercury, a known neurotoxin," explains IAOMT President Michael Rehme, DDS, NMD.  "Based on this science, we have strongly recommended that safety measures be enacted for dental procedures involving these silver-colored fillings, and we have also intensely advocated for the end of dental amalgam usage."