Today, Stryker's Interventional Spine business is all in—providing an extensive and innovative product portfolio for vertebral augmentation, radiofrequency ablation, bone tumor ablation and minimally invasive lumbar decompression procedures.
Our first vertebroplasty products are launched.
Single lesion RF generator is introduced.
MultiGen® radiofrequency generator with 4 lesion capability is launched.
Our first automatic mixer, AutoPlex®, and VertaPlex® bone cement are launched.
VertaPlex® HV PMMA bone cement is developed to address specific viscosity and working time preferences for treating vertebral compression fractures.
Our first kyphoplasty device, 10-guage iVAS® balloon system, is launched.
Venom® cannula and electrode system is launched, which delivers large lesions in a short amount of time.1,2
11-gauge iVAS® balloon system, available in 10mm and 15mm balloon sizes, is launched.
8-gauge iVAS® balloon system is launched.
VertePort X4 Manifold® cement delivery assistant and TroFlex curved needle is launched.
VertaPlex® HV bone cement becomes the first PMMA in the U.S. to receive 510(k) clearance for the fixation of pathological fractures of the sacral vertebral body or ala, using sacral vertebroplasty or sacroplasty.
CareFusion's vertebral compression fracture (VCF) portfolio, including the AVAFlex® balloon system, is acquired by Stryker.
AVAFlex® balloon system is launched for use with our bone cements and the AutoPlex® mixing and delivery system.
MultiGen® 2 RF generator, made for reliability, efficiency and ultimate control and customization, launches.
Vexim is acquired.
iVAS® Elite high-pressure balloon system (rated to 808 psi) is launched.
SAKOS pivotal trial results are released. This study demonstrated the non-inferiority of SpineJack® system to BKP and also established the superiority of SpineJack system over BKP with regards to reduced adjacent level fractures (ALFs) and restored midline vertebral body (VB) height at both 6 and 12 months after the procedure.3
SpineJack® system receives 510(k) clearance in the U.S. for treatment of osteoporotic vertebral compression fractures.
CMS grants new technology add-on payment (NTAP) for SpineJack® system, which provides eligible hospitals with incremental reimbursement for the SpineJack system for fiscal years 2021-2022 (October 1, 2020 to September 30, 2022).4,5
CMS grants transitional pass-through payment for SpineJack® system, which provides eligible outpatient settings and ambulatory surgery centers (ASCs) with incremental add-on payment for SpineJack system treatment due to substantial clinical improvement demonstrated over existing technologies.6
SpineJack® system receives 510(k) clearance in the U.S. for treatment of type A traumatic vertebral compression fractures with or without posterior instrumental fixation.
OptaBlate® bone tumor ablation system received 510(k) clearance in the U.S. for treatment of painful benign and metastatic bone tumors.
OmniCurve® unipedicular curved balloon system is released with enhancements to reach midline more reliably.7
SpineJack® system receives 510(k) clearance for the fixation of compression fractures that result from malignant lesions – myeloma or osteolytic metastasis.
Building on the gold standard you expect, the upgraded AutoPlex® M4 is adding control to the mix.
Vertos Medical, Inc. is acquired by Stryker, including the mild® procedure.
OptaBlate® Curve Probes receives 510(k) clearance for a unipedicular curved bone tumor ablation system.
OptaBlate® BVN System receives 510(k) clearance from the U.S Food and Drug Administration for basivertebral nerve ablation.
By continuously investing in research and technology, we provide advanced medical technology for interventional spine procedures. We aren’t settling with the current standard of care. We continually ask, “What if?” and “What’s next?”—because that’s where bolder approaches and improved outcomes begin.
The vision of IVS is to improve the life of patients with advanced percutaneous solutions that help treat chronic pain and restore mobility. Minimally invasive procedures such as vertebral augmentation procedures and radiofrequency ablation may help provide pain relief.
Guided by feedback from our customers, we’re creating advanced percutaneous solutions. We don’t just want to be your provider. We want to be a partner that helps you drive procedural efficiencies, pursue improved outcomes and expand into new procedures.
Thank you for your interest in Stryker's Interventional Spine products—bold and innovative approaches for treating patients experiencing pain. Tell us how we can help by answering the following questions, and we’ll work to get you what you need.
To place an order, contact your Stryker's Sales Representative or Stryker's Customer Service at 1 800 253 3210.
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