Dr. Stephen E. Robbins, MD

Dr. Stephen E. Robbins, MD
Spine

Education

• Abraham Lincoln School of Medicine, University of Illinois, Chicago, Illinois
• Certified, American Board of Orthopedic Surgery

Academic Appointments

• Attending staff, Columbia St. Mary's Hospital Milwaukee, St, Francis, Children's, St. Lukes, Sinai Samaritan, Milwaukee County Medical Complex, Milwaukee
• Clinical Instructor, Department of Orthopedic Surgery, Medical College of Wisconsin
• Clinical Instructor Dept. of Orthopedics, Medical College of Wisconsin
• Board Examiner, American Board of Orthopedic Surgeons

Abstracts / Papers

• Daniel Brodke, MD et al. "Prospective Randomized Trial of a New Anterior Lumbar Fusion Device". 15th Annual North American Spine Society Meeting, October 28,2000
• Paul M. Arnold, MD et al. "Multicenter Prospective Study of Clinical Outcomes of Lumbar Degeneration with PLIF Allograft Spacers”. Abstract, 1st Annual World Spine Conference, Chicago, IL August 10, 2003
• Henry LG, Cattey RP, Stoll JE & Robbins SE. "Laparoscopic Assisted Spinal Surgery.” Journal of Laparoscopic Surgeons, 1997
• Gertzbein SC et al. "Scoliosis Research Society: Multicenter Spine Fracture Study.” Spine, 1996
• Gertzbein SC, Betz R, Clements D, Errico T, Hammerberg K, Robbins S, Shepherd E, Weber A, Kerina M, Albin J, Wolk D, & Ensor K. "Semirigid Instrumentation of the Management of Lumbar Spinal Conditions combined with Circumferential Fusion: A Multicenter
  Study." Spine, 1996

Research Projects

• Clinical Investigator DePuy Spine, Johnson/Johnson Moss Miami SI Pedicle Screw Instrumentation Device
• Clinical Investigator for the Synthes Spinal Internal Fixator
• Clinical Investigator for the MOSS Spinal System
• Clinical Investigator for the BAK Interbody Fusion System for Spine Tech evaluating BAK/Laparoscopic Study for degenerative disk disease
• Investigator for the Multi-Center Trial for DePuy-Motech titanium lumbosacral fusions, IRB number 387
• Clinical Investigator for the Multi-Center Trial for the Synthes Titanium Interbody Spacer (TIS) Laparoscopic Clinical Study
• Clinical Investigator for the FDA Syncage Clinical Study
• Clinical Investigator for the Comparison of Autograft to DBX (Demineralized Bone Matrix Putty) with Autograft Used in Posterolateral Lumbar Fusion
• Clinical Investigator for the Sulzer/SpineTech BAK/C and Instrumented ACDF with Bone-A Prospective Outcome Assessment
• Clinical Investigator for the Clinical Outcomes of Lumbar DDD Treated with PLIF Allograft Spacers

Contact

Email Address: srobbins@milwaukeespinal.com
Website: www.drstephenrobbins.com