About this trial

This is a multicenter, prospective, retrospective, Post Market Clinical Follow-up (PMCF) study in subjects who have undergone or will undergo surgery utilizing one or more Stryker devices according to Stryker cleared Instructions for Use (IFU).

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Spinal Fusion
  • Spinal Fusion
  • Spinal Deformities Correction

Treatment groups

5,222 Participants
are divided into 3 treatment groups

Locations

7
Florida
Mayo Clinic Florida32224, Jacksonville United States
Maine
MaineHealth Neurosurgery and Spine04074, Scarborough United States
Michigan
Michigan Orthopaedic Surgeons48033, Southfield United States
Ohio
Cleveland Clinc44195, Cleveland United States

Sponsors and collaborators

VB Spine, LLC

Lead sponsor