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.

Advertisement

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.

More articles on devices:

Bacterin CEO’s strategy at work: 3 sales leaders join the team
Spine Wave nabs industry veteran Laine Mashburn as global marketing, business development exec

Globus Medical launches spinal deformity system

 

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

Advertisement

Next Up in Spinal Tech

Advertisement

Comments are closed.