Stenosis
For patients with lumbar spinal stenosis, the classic surgery is decompression (laminectomy or laminotomy). While effective, decompression alone can sometimes leave the spine less stable, leading to fusion. The Coflex® Interlaminar Stabilization® device offers an alternative: after decompression, a small implant is placed between the spinous processes to provide stability without eliminating motion. At Desert Spine and Pain, neurosurgeon Dr. David L. Greenwald, M.D., FAANS, FACS offers Coflex placement for properly selected patients, combining reliable decompression with motion preservation.
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In simple terms: Coflex is a small, titanium U-shaped device placed between the bones in your lower back after decompression. It holds the space open for nerves and stabilizes the spine without fusion.
Scientifically: The Coflex device is an interlaminar dynamic stabilizer implanted after lumbar decompression. It resists extension, maintains foraminal and canal dimensions, and redistributes load, providing stability while preserving sagittal motion at the treated level.
Lumbar spinal stenosis causing neurogenic claudication
Back and leg pain relieved by flexion (classic “shopping cart sign”)
Patients who fail conservative care (PT, medications, injections)
Single- or two-level stenosis (typically L1–L5) without instability requiring fusion
Good candidates:
Moderate lumbar stenosis confirmed on MRI/CT
No significant spondylolisthesis (>Grade 1)
Desire to avoid spinal fusion if possible
Intact spinous processes
Not candidates if:
Significant instability, deformity, or high-grade spondylolisthesis
Severe osteoporosis or prior laminectomy with spinous process removal
Multi-level disease beyond two levels
Anesthesia & positioning: You’re asleep under general anesthesia, lying face down.
Lumbar decompression: The lamina and ligamentum flavum are trimmed to relieve nerve pressure.
Implant placement: A small titanium U-shaped device (Coflex) is placed between spinous processes at the treated level.
Stabilization: The device locks in place, supporting the decompressed area while preserving motion.
Closure: The incision is closed; many patients go home the same day or next.
Exposure: Posterior midline or paramedian incision, tubular retractor system possible.
Decompression: Laminotomy/laminectomy ± medial facetectomy to free neural elements.
Sizing: Interspinous space sized using templates; implant chosen accordingly.
Implant insertion: Coflex device impacted between spinous processes; wings expanded to secure position.
Final check: Fluoroscopy verifies placement; device resists extension but allows flexion.
Closure: Layered closure; sterile dressing applied.
Provides stability without fusion
Preserves motion at the treated level
Faster recovery compared to fusion
Reliable relief of leg pain and neurogenic claudication
Less stress on adjacent levels compared to fusion
Device migration or loosening (rare with correct sizing)
Spinous process fracture (uncommon)
Infection, bleeding, or dural tear (as with any decompression)
Not appropriate for patients with instability, deformity, or osteoporosis
May still require conversion to fusion in the future if degeneration progresses
Day 0–1: Walking the same day; many go home within 24 hours
Weeks 1–2: Light activities, incision care, frequent short walks
Weeks 2–6: Desk work and driving usually resumed
6–12 weeks: Structured physical therapy; progressive return to activity
3–6 months: Strong symptom relief; most activities restored
12 months: X-rays confirm ongoing stability and motion preservation
Expert neurosurgeon: Dr. Greenwald is highly experienced in both decompression and motion-preserving procedures like Coflex
Personalized care: Careful patient selection ensures the best outcomes
Minimally invasive focus: Small incisions and precision tools for quicker recovery
Full-spectrum options: From decompression alone to Coflex to fusion, all tailored to your needs
Fusion eliminates motion at the treated level. Coflex preserves motion while providing stability after decompression.
It is best for patients whose primary issue is leg pain and walking intolerance from stenosis. Back pain relief is variable.
Device migration is rare when placed correctly. We use meticulous technique and proper sizing to minimize this risk.
Many patients resume light activities within 2–6 weeks, with full recovery by 3–6 months.
We emphasize evidence-based patient selection, advanced MIS decompression, and long-term monitoring to maximize safety and effectiveness.
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Phone: (602) 566-9500
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Conditions ,Treatments Surgery &Wellness
October 06, 2025•0 min read
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