Four Intracept system components displayed on blue gradient background.

The Intracept System

The only clinically proven, purpose-built system for vertebrogenic pain.1

System overview

The Intracept System enables a physician to effectively target and ablate the basivertebral nerve (BVN) to provide relief of vertebrogenic chronic low back pain (CLBP). The Intracept System includes purpose-built Intracept Access Instruments for creating a path to the BVN, proprietary radiofrequency (RF) ablation technology for effectively ablating the BVN, and comprehensive training and case support.

Predictable and precise

Explore the Intracept Access Instruments

Advancing the proven, durable and safe Intracept™ Procedure with next-generation basivertebral nerve targeting.

Gray medical handle tool labeled Intracept with slim shaft.

Bevel and Diamond Introducers

Gray surgical instrument with adjustable screw handle and long shaft.

Curved Cannula Assembly

Slim gray medical probe with rounded top and long shaft.

Straight Stylet

White and blue medical probe with narrow tip and ergonomic grip.

Intracept RF Probe

Intracept RF generator with attached probe and digital screen displaying data.

How the system works

Why choose Intracept?

Why choose Intracept

Minimally invasive and implant free

Why choose Intracept

Long-term pain relief 1

Why choose Intracept

Preserves overall spine structure

Why choose Intracept

Same day procedure; brief recovery

Why choose Intracept


2 weeks to 3 months for most patients to feel relief 2,4

Why choose Intracept

Proven safety profile*


The Intracept Procedure is supported by unparalleled clinical evidence, including two Level I RCTs

Results from multiple clinical trials demonstrate the Intracept Procedure is:

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Safe

Strong safety profile with less than 0.3% rate of serious device or procedure-related complications reported.*

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Effective

Two Level I RCTs demonstrate that the Intracept Procedure is an effective treatment compared to both a sham control procedure and to non-surgical standard care. 1,5

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Durable

Significant improvements in function and pain seen at 3 months post the Intracept Procedure are sustained more than 5 years after a single treatment.1


Discover more

Probe within a spinal vertebra during a minimally invasive procedure.

* Data on file.

  1. Fischgrund J, Rhyne A, Macadaeg K, et al. Long-term outcomes following intraosseous basivertebral nerve ablation for the treatment of chronic low back pain: 5-year treatment arm results from a prospective randomized double-blind sham-controlled multi-center study. Eur Spine J. 2020;29(8):1925-34. http://doi.org/10.1007/s00586-020-06448-x
  2. Fischgrund JS, Rhyne A, Franke J, et al. Intraosseous basivertebral nerve ablation for the treatment of chronic low back pain: a prospective randomized double-blind sham-controlled multi-center study. EurSpine J. 2018;27(5):1146-56. doi:10.1007/s00586-018-5496-1
  3. Smuck M, Khalil JG, Barrette K, Hirsch JA, Kreiner S, Koreckij T, et al. A prospective, randomized, multi-center study of intraosseous basivertebral nerve ablation for the treatment of chronic low back pain: 12-month results. Reg Anesth Pain Med. 2021;rapm-2020-102259. doi:10.1136/rapm-2020-102259
  4. Macadaeg, E. Truumees, B. Boody, E. Pena, J. Arbuckle II, J. Gentile, R. Funk, D. Singh, S. Vinayek, A prospective, single arm study of intraosseous basivertebral nerve ablation for the treatment of chronic low back pain: 12-month results, North American Spine Society Journal (NASSJ) (2020), doi.org/10.1016/j.xnsj.2020.100030
  5. Koreckij T, Kreiner S, Khalil JG, Smuck M, Markman J, Garfin S. Prospective, randomized, multicenter study of intraosseous basivertebral nerve ablation for the treatment of chronic low back pain: 24-month treatment arm results. NASSJ. Published online October 26, 2021. DOI: https://doi.org/10.1016/j.xnsj.2021.100089

CAUTION: The law restricts these devices to sale by or on the order of a physician. Indications, contraindications, warnings, and instructions for use can be found in the product labelling supplied with each device or at www.IFU-BSCI.com. Products shown for INFORMATION purposes only and may not be approved or for sale in certain countries. This material not intended for use in France.