WORLD’S 1ST ROBOTIC ARTICULATING DECOMPRESSION SYSTEM
FDA 510(K) CLEARED • CE MARKED • ISO 13485
PATENTED 10-WAY 3D ARTICULATION
Antalgic-Trak® Deluxe Robotic Spinal Decompression & Range-of-Motion System
Engineered by Spinetronics USA and co-invented by Dr. David Bass and Dr. Scott Denny, Antalgic-Trak® represents the first major evolutionary breakthrough in non-surgical spinal decompression in 50 years. Transcending rigid, one-dimensional “flat-table” systems, Antalgic-Trak delivers patented 10-way cervical and lumbar articulating motion during active decompression. This enables clinicians to posture-target herniations, decompress spine segments in their antalgic pain-relief vectors, and restore Range of Motion (ROM) through computerized Kinetic Decompression-Mobilization (KDM).
15 Peer-Reviewed Papers
Interactive Video Cinema & Treatment Masterclass
Click any video below to launch instant high-definition clinical playback with full controls.
Featured Clinical Demonstrations: Cervical & Lumbar Articulation in Motion
Section A: Clinical Keynotes & Case Study Presentations
Section B: Physician Masterclass & Patient Education Series (Vimeo Master Series)
Section C: Hands-on Clinical Setup & Interface Navigation Guides
The Multi-Axis Revolution: Why Linear “Flat Cable Tables” Fall Short
For over 50 years, motorized traction relied on straight, linear cable pull tables. While linear pulling can influence parallel longitudinal fibers, human spinal pathology is inherently three-dimensional. Disc bulges and herniations frequently present lateralization, foraminal migration, and rotatory torque that cannot be addressed in a rigid flat supine posture.
Parallel Muscle Fibers (1D Tension)
Longitudinal muscles such as the Erector Spinae run parallel to the vertebral column. Conventional traction exerts tension along this single vector, but accounts for only a fraction of deep paraspinal stabilization.
Angled & Rotational Fibers (3D Articulation)
Deep stabilizer groups—including the Multifidus, Rotatores, Sacrospinalis, and Interspinales—run obliquely and perpendicularly. They require precise lateral flexion and axial rotation under tractive elongation to release spasm and facilitate annular healing.
Antalgic Posture Matching
Acute disc herniation patients present with an “antalgic lean”—a protective posture that relieves root pressure. Antalgic-Trak allows clinicians to position the patient directly into their antalgic relief posture before initiating decompression, eliminating patient guarding and reflex spasm.
Clinical Indications & Treatment Scope
Antalgic-Trak® is FDA 510(k) cleared and CE certified for the comprehensive non-surgical rehabilitation of chronic, acute, and radiating spine disorders:
Published Clinical Evidence & Multidisciplinary Research
Antalgic-Trak® technology is backed by prospective clinical trials, independent hospital outcome studies, and peer-reviewed spinal decompression literature:
Technical Specifications & System Capabilities
| Parameter | Specification |
|---|---|
| Model Designation | Antalgic-Trak® Deluxe Robotic Spinal Decompression System (Robotic-ATT) |
| Decompression Modes | Static, Intermittent, Articulating Cyclic, Progressive Ramp, Regressive Ramp, Dynamic ROM |
| Articulation Range | 10-Way Patented 3D Articulation: Flexion, Extension, Bilateral Lateral Bending, Bilateral Axial Rotation |
| Lumbar Traction Force | Computer controlled up to 200 lbs (90.7 kg) with load-cell precision feedback |
| Cervical Traction Force | Computer controlled up to 50 lbs (22.7 kg) with micro-increment calibration |
| Patient Mounting System | Upright neutral seated chair mount with motorized transition to horizontal therapy posture |
| Torso Stabilization | Patented dual axillary (underarm) rigid supports & clinical harness system (zero chest constriction) |
| User Interface | Medical-grade full-color Touchscreen GUI with digital therapy logging & custom protocol presets |
| Safety & Compliance | Patient Emergency Stop Switch, Dual Optical Safety Sensors, Clinician Manual Release, Motor Over-Torque Guard |
| Regulatory Clearances | FDA 510(k) Cleared Medical Device, CE Mark Medical Devices Directive, ISO 13485 Certified |
| Mobility & Construction | Heavy-duty steel chassis with 4 extra-large lockable swivel casters; optional Lucite perimeter floor platform |
| Electrical Specifications | 100–240 VAC, 50/60 Hz universal medical power supply |

















Reviews
There are no reviews yet.