Quick Study Video

Cervical Fusion with CORUS™ PCSS

This video provides the essentials for Tissue-Sparing Posterior Cervical Fusion with CORUS™ PCSS.
Includes talks by expert surgeons and clinical investigators.
FDA-cleared with Level-1 data.

What you'll learn

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What You'll Learn

Tissue-Sparing Circumferential Cervical Fusion for High-Risk Patients

High-risk patients present with multilevel disease, risk factors for pseudarthrosis, and/or complex clinical profiles.

Clinical Evidence on the Treatment of Multi-Level Cervical Fusion

This includes a review of the landmark FUSE Study, the largest randomized, prospective study to evaluate 3-level cervical fusion.

Surgical Technique Demonstration

C-Arm setup and imaging tips.
Incision planning and trajectory mapping.
Tissue-sparing technique for joint access, decortication, and bone graft delivery.

Case Studies & Real-World Outcomes

Explore compelling case studies showcasing the clinical value of this approach. See how surgeons and patients are benefitting from our technology.

Watch Now: CORUS PCSS Quick Study

Over

2,300

Spine Surgeons Trained

Over

21,000

Surgical Cases Performed

Approved at over

2,600

Hospitals & Facilities

CORUS™ PCSS has become the fastest-growing technology for cervical spine surgery

Superior Fusion Outcomes Faster.12 months after surgery, patients treated with ACDF & CORUS PCSS demonstrated a clinically superior fusion rate compared to ACDF alone.¹
Reduces Reoperation Rates.More than one in five 3-level ACDF patients require revision surgery within 24 months. Nonunion (symptomatic pseudarthrosis) is the #1 reason.¹
Superior Safety Outcomes.Patients treated with ACDF and PCSS patients achieved greater composite safety success at 12 and 24 months than patients treated with ACDF alone.¹

Learn more about CORUS™ PCSS

Frequently Asked Questions

How do most spine surgeons train on this technology?

Anatomical model training and surgical simulation are the most popular training modalities for spine surgeons and neurosurgeons and valued for their convenience. Both options allow for effective, hands-on training at your O.R. or office and make it easy to add training sessions to busy schedules.

Which patients may benefit from this technology and what are the criteria  for patient selection?

We specifically cover patient selection during training because spine surgeons are often curious about which patients are good candidates for this technology. Understanding the indications and contraindications for tissue-sparing posterior fusion is crucial for patient safety and optimal outcomes.

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About Providence Medical Technology

Our Purpose is to improve clinical outcomes for high-risk patients and prevent surgical failures of the cervical spine.

Our Mission is to establish Circumferential Cervical Fusion (CCF) as the standard of care for high-risk patients.

INDICATIONS FOR USE, CORUS PCSS LevelOne

A. CORUS Spinal System-X:
The CORUS™ Spinal System-X is a set of instruments indicated to be used to perform posterior cervical fusion in patients with cervical degenerative disc disease.

B. CORUS PCSS Implant:
CORUS™ PCSS is posterior spinal instrumentation with integrated screw fixation intended to provide immobilization and stabilization of spinal segments.
CORUS PCSS is placed through a posterior surgical approach in up to 3 consecutive levels of the cervical spine (C3-C7) and achieves bilateral facet fixation by spanning the facet interspace at each level with points of fixation at each end of the construct.

CORUS PCSS is intended as an adjunct to posterior cervical fusion (PCF) and is only intended to be used in combination with an anterior
cervical discectomy and fusion (ACDF) at the same level(s).

CORUS PCSS is indicated for skeletally mature patients with degenerative disc disease (DDD). DDD is defined as radiculopathy and/or myelopathy, neck and/or arm pain of discogenic origin as confirmed by radiographic studies.

CORUS PCSS is to be used with autogenous bone and/or allogenic bone graft.

C. DiViNE Portal System:
DiViNE™ Portal System is a set of instruments indicated to make the interior of a joint visible and/or to perform surgery within a joint.

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