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Relievant Medsystems Announces $70M Financing to Accelerate U.S. Commercialization of Intracept Procedure
Financing to build on significant 2020 commercial momentum following the publication of 5-year data demonstrating the long-term clinical benefits of the Intracept Procedure.
Relievant Announces Positive 12-Month Intracept Effectiveness Study Results From Community Based Practices
Relievant Medsystems, a privately-held medical device company transforming the treatment of Chronic Low Back Pain (CLBP), today announced the North American Spine Society Journal publication of results from an effectiveness study showing that the significant improvements in function and pain initially reported at an interim analysis of three months following the Intracept Procedure remained significant through one year.
Relievant Announces Publication of 5-Year Data Demonstrating Long Term Clinical Benefits of the Intracept Procedure in Chronic Low Back Pain Patients
Relievant Medsystems, a privately-held medical device company transforming the treatment of Chronic Low Back Pain (CLBP), today announced European Spine Journal publication of long-term data from the Level I SMART trial showing durability of improvements in pain and function beyond 5 years for patients treated with the Intracept procedure…
Relievant Announces Publication of Positive Results from Multi-Center Study of the Intracept® Procedure in Real-world Setting for Patients with Chronic Low Back Pain
Relievant Medsystems, a privately-held medical device company transforming the treatment of Chronic Low Back Pain (CLBP), today announced the publication of significant and clinically-meaningful outcomes from a prospective, open-label, single-arm, multi-center study in the European Spine Journal…
Relievant Announces Publication of Level l INTRACEPT Study
Relievant Medsystems, a privately-held medical device company focused on transforming the treatment of Chronic Low Back Pain (CLBP), today announced the publication of the Level I INTRACEPT Study results in The Spine Journal. The INTRACEPT Study is a Level I,...
Relievant Announces Publication of SMART Trial 24-Month Results
Relievant Medsystems, a privately-held medical device company developing minimally-invasive solutions for chronic low back pain (CLBP), today announced the publication of 24-month results from the SMART trial in the International Journal of Spine Surgery. A total of...
American Society of Spine Radiology Announces the Presentation of Results From the Level l INTRACEPT Study
Results from the pre-specified interim analysis of the landmark INTRACEPT randomized controlled trial were presented for first time on February 20, 2019 at the American Society of Spine Radiology (ASSR) meeting in Miami, Fla. The study demonstrated statistically and...
Relievant Announces Level l INTRACEPT Study Stopped Early for Superiority
Relievant Medsystems, a privately-held medical device company, developing minimally-invasive solutions for chronic low back pain (CLBP), today announced that a pre-specified interim analysis of the Level I INTRACEPT Randomized Controlled Trial (RCT) found a highly...
Relievant Announces Reimbursement Codes and APC Assignment for The Intracept® Procedure
Relievant Medsystems, a privately-held medical device company developing minimally-invasive solutions for chronic low back pain (CLBP), today announced that the Centers for Medicare & Medicaid Services (CMS) has established Healthcare Common Procedure Coding...
Relievant Announces First Commercial Intracept Procedures
Relievant Medsystems, a privately-held medical device company developing minimally-invasive solutions for chronic low back pain (CLBP), announced today the successful completion of the first commercial Intracept Procedures. The procedures were performed by Dr. Bradly...
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That’s Living
Proof.
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Welcome to the proof
of Intracept
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Key Findings:
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Key Findings:
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The Data Is Living Proof Too
Fewer Opiods
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Fewer Opiods
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Fewer Opiods
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Intracept Quick Facts
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How we’re living the proof.
Now in Effect: New Category | CPT Codes
Intracept Long Term Outcomes
New Patient Story
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Indications (Global)
As with any surgical procedure, there are risks and considerations associated with the Intracept Procedure. See important safety information below.
Physicians: See Indications, Contraindications, and Risks
Indications for Use: The Intracept™ Intraosseous Nerve Ablation System is intended to be used in conjunction with radiofrequency (RF) generators for the ablation of basivertebral nerves of the L3 through S1 vertebrae for the relief of chronic low back pain of at least six months duration that has not responded to at least six months of conservative care, and is also accompanied by features consistent with Type 1 or Type 2 Modic changes on an MRI such as inflammation, edema, vertebral endplate changes, disruption and fissuring of the endplate, vascularized fibrous tissues within the adjacent marrow, hypointensive signals (Type 1 Modic change), and changes to the vertebral body marrow including replacement of normal bone marrow by fat, and hyperintensive signals (Type 2 Modic change). Contraindications - Use of the Intracept Intraosseous Nerve Ablation System is contraindicated in: Patients with severe cardiac or pulmonary compromise, patients with active implantable pulse generators (e.g. pacemakers, defibrillators), patients where the targeted ablation zone is < 10 mm away from a sensitive structure not intended to be ablated, including the vertebral foramen (spinal canal), patients with active systemic infection or local infection in the area to be treated, patients who are pregnant, and/or skeletally immature patients (generally ≤ 18 years of age). Refer to the Instructions for Use provided with the Intracept Procedure or www.relievant.com/intracept/ for potential adverse effects, warnings, and precautions prior to using this product.
Caution: U.S. Federal law restricts this device to sale by or on the order of a physician.
Copyright © 2025 by Boston Scientific Corporation or its affiliates. All rights reserved.
Patients: See the Indications & Risks Involved
Contraindications include being pregnant, having weakened cardiac or pulmonary function, having an active implanted electronic medical device in the body (such as a pacemaker or defibrillator), being diagnosed with a systemic or local infection, or having an anatomy that could be damaged unintentionally while ablating the basivertebral nerve (based on your physicians’ clinical review). The Intracept Procedure is also contraindicated in patients who are skeletally immature – which generally means individuals under the age of 18 are not candidates. There are also certain risks and precautions regarding the procedure which you should be aware of before proceeding. Talk with your doctor about what indicates, and contraindicates, certain patients for the Intracept Procedure – as well as the risks and precautions for the procedure. For complete indications for use, contraindications, warnings, precautions, and side effects visit www.relievant.com/intracept/.
Caution: U.S. Federal law restricts this device to sale by or on the order of a physician.
Copyright © 2025 by Boston Scientific Corporation or its affiliates. All rights reserved.
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Physicians
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Intracept Long Term Outcomes
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New Patient Story
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Carousel Doctor
What Physicians Are Saying About Intracept
Brian Durkin, DO
NY Health,
Port Jefferson Station, NY
“If I see people with Modic changes I say, 'that's probably where your back pain is coming from. It's probably your vertebrogenic endplate changes that are causing your back pain.' So that's been a big change in our algorithm. We'll see patients for the first time and see if we can get them in the portal and treated.”
Kiran V. Patel, MD
Director, Neurosurgical Pain, Lenox Hill Hospital, NY
“For the right patient with lower back pain, the Intracept procedure is life changing. Of all of the procedures that I perform, it has delivered the most dramatic results for my patients.”
Casey Muir, MD
Southwest Spine and Pain Center,
St George, UT
“This is an exciting new treatment option for a type chronic low back pain that we haven't had a solution. Intracept treats focal low back pain that occurs from degeneration of the intervertebral discs causing vertebrogenic back pain. This pain stays in the low back and generally gets worse with bending forward. If you have these back pain features Intracept may be the solution to your back pain.”
David Tran, MD
Axion Spine & Neurosurgery,
Alpharetta, GA
“Intracept is an innovative, safe, and highly effective treatment for chronic low back pain. Patients can see dramatic, lasting improvements from this minimally invasive procedure, with little post-procedure pain and quick recovery time.”
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Looking for proof?
Hear from the ones living it.
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Video Grid
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Kourtney’s Story
“My best friend said to me, I have not heard you talk about your back in so long.”
Story
Debbie’s Story
Multiple injections, multiple failed
approaches—nothing worked.
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Next Step forms
Access Instruments CTA
The Intracept® System:
Now with Next-Generation Access Instruments
