Focus Medical / Motion Preservation
Synergy Spine Solutions

Synergy Disc®

Cervical Artificial Disc Replacement

FDA PMA-approved cervical ADR with mobile center of rotation. Preserves motion at the treated level — eliminating the adjacent segment degeneration associated with fusion. UHMWPE core and titanium endplates engineered for long-term durability.

22°
F/E ROM
±12°
Lateral Bend
PMA
Approved
FDA PMA · MRI Compatible
Synergy Disc Cervical Artificial Disc Replacement

Synergy Disc®

Cervical Artificial Disc Replacement

5mm Core
6mm Core
Manufacturer
Synergy Spine Solutions
FDA PMA Approved
Mobile COR
MRI Compatible
UHMWPE + Titanium

Key Differentiator

Preserve Motion.
Prevent Adjacent Segment Disease.

Cervical fusion transfers stress to adjacent segments, accelerating degeneration above and below the operative level. The Synergy Disc® maintains natural motion at the treated level with a mobile center of rotation — biomechanically closer to the native disc than fixed-core alternatives.

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Mobile Center of Rotation

Dynamic COR replicates the biomechanics of the native disc — distributing load more naturally than fixed-COR designs that alter motion patterns.

0° and 6° Lordotic Core

Two lordotic options accommodate different patient anatomy and cervical curvature requirements — matching the disc to the patient, not the patient to the device.

Anterior Translation

2mm A/P translation provides a kinematic degree of freedom that fixed-core ADR and fusion eliminate — preserving gliding motion through the full arc of movement.


Product Features

Advanced Biomechanics. Long-Term Durability.

FDA PMA Approved

Pre-market approval is the most stringent FDA review pathway — reserved for devices with the most significant risk. The Synergy Disc has met this highest standard.

Mobile Center of Rotation

Dynamic COR moves with the segment during motion — more closely replicating native disc biomechanics than fixed-COR designs that constrain the motion arc.

22° Flexion/Extension ROM

22° flexion/extension, ±12° lateral bending, ±12° axial rotation, and 2mm A/P translation — a comprehensive motion envelope that supports full cervical function.

UHMWPE + Titanium Construction

Ultra-high molecular weight polyethylene bearing surface paired with titanium endplates delivers the combination of low friction, durability, and osseointegration required for long-term performance.

MRI Compatible

Full MRI compatibility means patients can undergo post-operative imaging without device interference — critical for ongoing monitoring of adjacent segments and neural structures.

Commercial Availability (AU/EU/CA)

Commercially available in Australia, Europe, and Canada, with US availability through FDA investigational pathway. An established international track record of clinical success.


Clinical Applications

When to Consider Synergy Disc®

Single or two-level cervical disc disease (C3–C7)
Symptomatic radiculopathy unresponsive to conservative treatment
Patients preferring motion preservation over ACDF
Adjacent segment disease prevention (post-fusion)
Myelopathy from disc herniation or osteophytes

Motion vs. Fusion

ADR preserves motion at the operative level and reduces the mechanical stress transferred to adjacent segments — the primary cause of long-term adjacent segment degeneration seen with fusion.


Specifications

Product Specifications

Device Synergy Disc® Cervical ADR
Materials UHMWPE + Titanium Endplates
Core Options 0° and 6° Lordotic
Heights 5mm and 6mm
F/E ROM 22° Flexion/Extension
Lateral Bend ±12°
Axial Rotation ±12°
A/P Translation 2mm
MRI Compatible Yes
FDA Status PMA Approved (Investigational US)
Manufacturer Synergy Spine Solutions

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Ready to Add Synergy Disc®
to Your Cervical Program?

Focus Medical Corporation is the authorized distributor for Synergy Spine Solutions. Contact us to discuss availability, pricing, and clinical support for your cervical spine program.

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