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An Open, Parallel-group, Randomized, Medical Device Study to Assess the Usability and Performance of Surgify HaloTM in Spine Surgery Versus State-of-art (Rosen Burr)

Who can join

Ages 21 to 85 · All sexes

Inclusion Criteria:

* Disease of the spine requiring surgery with bone removal

  * Ability to understand the purpose and risks of the study and to give written informed consent
  * Age 21-85 years

Exclusion Criteria:

* Abnormalities of bone tissue
* Vulnerable patients (such as prisoners, Individuals with limited or no reading skills, decisionally impaired persons, persons in nursing homes, patients in emergency), and pregnant women
* Allergy or hypersensitivity to medical-grade stainless steel or any alloying components
* Problems with blood clotting

About the study

The purpose of this research study is to:

test the usability and performance of the medical device Surgify Halo ™ in spine surgery test the level of "chattering " during the use of the device test the cutting performance of Surgify Halo™in comparison to the usual drill bit used in spine surgery ( Rosen burr).

This medical device is available for its indications for shaping and removal of hard tissue and bone in neurosurgical, spinal, ENT, and general surgical procedures.

The target is to enroll 30 participants in this study.

What is being tested

• A burr used in spine surgery (device)

Sponsor: Surgify Medical Oy · Participants: 30 · Started: Feb 19, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT06827795

Locations in the U.S.

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.