CTL Medical receives FDA clearance for ACIF cage with TiCro technology: 4 key notes

Surface Technology

CTL Medical obtained FDA clearance and approval for the Matisse Ti-PEEK ACIF Cage system with TiCro technology.

Here are four things to know:

 

1. The cage is made with CTL Medical's proprietary TiCro surface technology, which is designed to increase bone ingrowth with titanium and PEEK.

 

2. The updated Ti-PEEK interbody offers surgeons 200 percent greater endplate contact surface area in addition to geometric surface morphology for increased mechanical locking at the cage and bone interface.

 

3. The device has a tapered leading edge that eases insertion as well as a large graft area to promote bony fusion. It's available in a variety of sizes and configurations.

 

4. Matisse Ti-PEEK Cage with TiCro is indicated for skeletally mature patients with degenerative disc disease in the cervical spine and radicular symptoms at one disc level.

 

"The Matisse device line now offers three material options to satisfy surgeons and their patients' ever-changing needs," said Vice President of Marketing for CTL Medical Rose Moore. "As with previous models, the Matisse Ti-PEEK system offers streamlined instrumentation and a variety of footprints, heights and lordotic profiles to accommodate variation in patient anatomy."

 

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