Camber Spine FDA 510(k) Clearance for Siconus SI Joint Fixation

Camber Spine Technologies received FDA 510(k) clearance for the Siconus™ SI Joint Fixation System for the treatment of sacroiliac disease, as a complement to Prolix™ custom-machined allograft.

Siconus was developed under a collaborative agreement with the Institute for Musculoskeletal Science & Education.

Camber Spine received its...

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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