Meditech Spine's next-generation Talos device earns FDA clearance: 4 things to know

Spinal Tech

The FDA cleared Meditech Spine's Talos Lumbar (HA) Peek IBF.

Here are four things to know:

 

1. An intervertebral body device, Talos is designed to help treat degenerative disc disease of the lumbar spine in patients with up to Grade 1 spondylolisthesis at one or two contiguous levels from L2 to S1.

 

2. Surgeons may use the device with autograft or allograft made of cancellous or corticocancellous bone graft.

 

3. Meditech will market its Talos lumbar interbody line with Invibio Biomaterial Solutions, PEEK-OPTIMA HA Enhanced material.

 

4. U.S. surgeons have used the Talos Peek Lumbar IBF devices since 2010.

 

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