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Amedica Corp. lands FDA 510(k) clearance for a 2nd generation interbody fusion device system.

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Amedica Corp. won FDA 510(k) clearance for a 2nd generation of the company's cervical and lumbar interbody fusion devices (IBF).

The Utah- based spinal and reconstructive medical device manufacturer said the devices, which are made with a proprietary silicon nitride biomaterial, could help surgeons perform minimally invasive procedures when conducting lumbar lateral interbody fusion (LLIF).

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