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The Prodisc-L total disc replacement has been determined to be safe and effective in the treatment of degenerative disc disease (DDD) in the lower back.  The Prodisc-L total disc replacement surgery is intended to:

 

Remove the diseased disc
Restore normal disc height
Significantly reduce discogenic pain
Preserve motion in affected vertebral segment
Improve patient function

 

The ProDisc-L total disc replacement is clinically proven to maintain motion in the spine.


Design Philosophy

The Prodisc-L implant has been designed to maintain the physiological range of motion in the spine. The implant was developed using the clinically proven ball and socket concept used in joint replacement implants for over 40 years. The Prodisc-L implant is composed of three components – two cobalt chrome alloy (CoCrMo) endplates and an ultra-high molecular weight polyethylene (UHMWPE) inlay.

 

The key features of the Prodisc-L design philosophy are:

 

Ball and socket design

Controlled and predictable motion
Secure fixation of polyethylene inlay with fixed center of rotation
Semi-constrained design based on ball and socket joint principle
Prevents pure anteroposterior shear to protect posterior structures  

 

Secure fixation

Patented central keel and lateral spikes provide secure primary fixation
Plasma sprayed titanium coating promotes bony on growth.

 

Modular implant components

Different anatomical combinations facilitate an accurate match with the patient’s anatomy
- Medium and large footprints
- 10, 12 and 14 mm heights  (posterior height)
- 3°, 6°, 9° and 11º lordotic angles

 

Safe and reproducible surgical technique

Three-step implantation technique
Enables accurate sizing and placement of the implant

 

Straightforward instrumentation

Designed for midline anterior approach
Enables clear visualization into the disc space
Minimizes exposure and risk of damage to vascular structures

Surgical Technique

Synthes has worked with leading spine surgeons from around the world to refine the Prodisc-L instrumentation and surgical technique to facilitate safe and reproducible implantation through a midline anterior approach.

 

The Prodisc-L surgical technique, instrumentation, and implant function as a unified system.  The instrumentation has been engineered to enable precise placement and visualization of the implant.  The trial and chisel size and placement correspond exactly to the final implant size and placement. All instrumentation is contained within the medial-lateral width of the implant, minimizing the size of the incision and amount of vascular retraction required for implantation.





 
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