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Our solutions in Neurosurgery

StealthStation™ S8

Surgical navigation system

The StealthStation™ S8 surgical navigation system offers both optical and electromagnetic tracking capabilities.

Stealth
Autoguide™

Cranial robotic guidance platform

Stealth Autoguide™ cranial robotic guidance platform aligns to your surgical plans for cranial procedures.

MidasRex™
MR8™

High-speed drill system

Midas Rex™ MR8™ offers lower operating temperature, less chatter, improved visibility of the surgical site and even better cutting performance.^1-8

Navigable with StealthStation™ S8, it seamlessly integrates with other technologies in our portfolio.

StrataMR™ II

Adjustable pressure valve

Designed for the treatment of hydrocephalus, the StrataMR™ II adjustable pressure valve offers simplicity, durability, and ease of use in implantation and adjustment — plus MRI resistance.

Visualase™

The Visualase™ MRI-guided minimally invasive laser ablation system allows monitoring of the tissue ablation in real-time.

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References

Based on 10200261DOC_RevR_FINAL: UN0216-Validation: 10863177DOC MR8 Stealth-Midas Design Validation; UN0020: 10822457DOC MR8 Design Validation; UN0087 -The drill platform needs to provide surgeons precise control for the INTENDED USE., UN0471: The drill platform needs to provide surgeons with Sensory Feedback while drilling.
Based on 10822457DOC MR8 Design Validation.
Based on 10896051DOC MR8 Design Validation Test Report.
Based on 10862768DOC MR8 NAVIGATED ELECTRIC MOTOR RELIABILITY (CCA) DESIGN VERIFICATION.
Based on 10623499DOC MR8 Electric Motor CCA.
Based on 10891453DOC MR8 Electric Motor Product Life Design Verification Report.
Based on MR8 Modeling & Simulation Review - FTW - 10Dec2015.
Based on 10832428DOC - MR8 Telescoping technical review meeting minutes conducted on July 18 2018. (See MR8 TT DCTR July 2018.pptx Slide 4).

This material should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s). Please note that the intended use of a product may vary depending on geographical approvals.

See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events.

For a MRI compatible device(s), consult the MRI information in the device manual(s) before performing a MRI. If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com.

Manuals can be viewed using a current version of any major internet browser.

For best results, use Adobe Acrobat® Reader with the browser. Medtronic products placed on European markets bear the CE mark and the UKCA mark (if applicable). For any further information, contact your local Medtronic representative and/or consult Medtronic’s websites.