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FDA clears Meditech Spine's intervertebral body device

Meditech Spine obtained clearance from the FDA for its Talos Lumbar (HA) Peek IBF, an intervertebral body device for patients with lumbar degenerative disc disease who have up to grade 1 spondylolisthesis at one or two contiguous levels from L2 to S1. The device may be used with autograft or allograft composed of corticocancellous or cancellous bone graft.

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