-

VySpine Announces FDA Clearance for ClariVy Cervical IBF System

TALLAHASSEE, Fla.--(BUSINESS WIRE)--VySpine, a spine innovation leader using differentiated materials and designs, announced today that it has received 510(k) clearance from the FDA for the its ClariVy Cervical IBF System which is designed for use in anterior cervical discectomy with fusion (ACDF) procedures.

The ClariVy Cervical IBF System features cervical interbody fusion devices made from either PEEK Optima LT1, or PEEK Optima HA-Enhanced. PEEK Optima LT1 has been the standard for interbody devices for decades, featuring radiolucency and a modulus of elasticity close to that of natural bone. PEEK Optima HA-Enhanced has embedded Hydroxyapatite fibers to create better bony apposition to the implant.

“The ClariVy Cervical IBF System is the first in a series of differentiated interbody systems being developed by VySpine,” said Tom McLeer, CEO of VySpine. “Using new materials and creative surgeon input, we are building exceptional quality, flexibility, and pricing into all our products. This is just the next step in a series of exciting, innovative product launches scheduled for 2022.”

The ClariVy Cervical IBF System is offered in numerous footprints and heights, ranging from 4mm to 11mm and available either with or without locking screws. Additionally, the ClariVy implants are available in a range of lordosis. The ClariVy Cervical IBF System also features IBF-S implants, which have self-drilling screws to aid in anchoring the device directly to the bone. These screws are self-locking to ensure quick and easy fixation.

About VySpine

VySpine was created through active internal development and the licensing of various proven technologies using innovative materials and designs. This comprehensive line of core spine products and newly developed specialty products allow us to meet the needs of both health care providers and surgeons. The company strives to outpace the competition by collaborating with key spine innovators while providing a flexible, cost-effective approach to spine care. Learn more at vyspine.com

“VySpine” and “ClariVy” are registered trademarks of VySpine.

“PEEK Optima” is a registered trademark of Invibio Biomaterial Solutions.

Contacts

Paul Williams, 310-569-0023, paul@medialinecommunications.com

Industry:

VySpine

Release Summary
VySpine has received FDA clearance for its ClariVy Cervical IBF System.
Release Versions
English
Hashtags
#ClariVy
#FDA
#cervicalIBF
#vyspine

Contacts

Paul Williams, 310-569-0023, paul@medialinecommunications.com

More News From VySpine

Vy Spine Announces FDA Clearance of 3D Printed LumiVy OsteoVy PEKK Lumbar IBF

BOUNTIFUL, Utah--(BUSINESS WIRE)--Vy Spine, a spine innovation leader using differentiated materials and designs, announced today that it has received U.S. Food and Drug Administration (FDA) clearance for its LumiVy OsteoVy PEKK Lumbar IBF. The device is indicated for intervertebral body fusion for use at either one level or two contiguous levels in the lumbar spine, from L2 to S1, for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. The LumiVy OsteoVy PEKK...

Vy Spine Announces FDA Clearance for its ClariVy OsteoVy PEKK Cervical IBF

TALLAHASSEE, Fla.--(BUSINESS WIRE)--Vy Spine, a spine innovation leader using differentiated materials and designs, announced today that it has received U.S. Food and Drug Administration (FDA) clearance for its ClariVy OsteoVy PEKK Cervical IBF, indicated for intervertebral body fusion for use at one level in the cervical spine, from C3 to T1, for the treatment of degenerative disc disease (DDD). The novel ClariVy OsteoVy PEKK Cervical IBF device combines the osseointegration properties of the...

VySpine Announces FDA Clearances for VySpan, VyLam and VySpine Innovations

TALLAHASSEE, Fla.--(BUSINESS WIRE)--VySpine, a spine innovation leader using differentiated materials and designs, announced today that it has received a trio of U.S. Food and Drug Administration (FDA) clearances for its products, providing increased diversity to the company’s portfolio. Among the approvals announced is FDA clearance for additional connectors for the VySpan PCT system to add to its versatility. These new, robust connectors can be easily attached to the VyLink Screw System. VySp...
Back to Newsroom