LorX® ALIF Titanium Cage is a posterior intracorporeal fusion device used for the correction and stabilization of the lumbar spine (L2 - S1) region for the treatment of lumbo-sacral spine diseases.

LorX® ALIF Titanium Cage is designed to be used two pieces in per level.

 

LorX® TLIF Titanium Cage is designed to be used with auxiliary spinal fixation systems (posterior screw-rod systems, anterior plate systems, anterior screw-rod systems, etc.) and is not recommended for use by itself.

 

The LorX® ALIF Titanium Cage is indicated at a maximum of two levels for patients who meet the indications and have adequate spinal strength.

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INDICATIONS:

LorX ALIF Titanium Cage is indicated for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with the degeneration of the disc confirmed by historical and radiographic studies. The device system is designed in order to get  to used easily with an autograft to facilitate additional fixation and fusion.

 

CONTRAINDICATIONS:

Contraindications include but are not limited to:

• Any medical or surgical condition that prevents the potential benefits of spine surgery, pathological obesity, pregnancy, overwhelming osteoporosis, open wounds, extreme local inflammation, drug and / or alcohol addiction, mental illness, extreme old age, body sensitivity to implant material, and / or allergy that preclude the potential benefits of spine surgery , acute or chronic infections, lack of patient cooperation.