SpineEx receives FDA clearance for personalized lateral lumbar cage: 3 things to know

Surface Technology

SpineEx earned FDA 510(k) clearance for its Sagittae lateral lumbar interbody fusion device.

Here are three things to know:

1. Sagittae is a personalized, adjustable expandable LLIF device designed to minimize impaction, maximize indirect decompression and provide a large graft space for lumbar fusion procedures.

2. It is designed for up to eight millimeters of continuous in situ expansion, with up to 30 degrees of continuous in situ lordotic adjustment. The large single graft chamber can be filled with bone graft material after insertion.

3. The new lateral cage is intended to minimize the need to forcefully impact the cage into the disc space, according to SpineEx Executive Chairman and CEO Roy Chin.

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