Precision Spine’s cervical interbody fusion device receives FDA clearance

 
Precision Spine received 510(k) clearance from the U.S. Food and Drug Administration and launched its VAULT-C Anterior Cervical Interbody Fusion Device.

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The VAULT-C is a stand-alone cervical interbody device intended for use in adult patients with degenerative disc disease of the cervical spine (C3-T1) at one disc level. It includes a plate/cage integrated design that allows for rigid screw fixation using a zero profile construct. It is also available in various heights and geometric footprints.

Precision Spine is a privately held medical device company focusing on spine product development.

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