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200+ spine medtech FDA clearances in 2023

The Food and Drug Administration cleared more than 200 spine-related devices and technologies with 510(k) approval in 2023.

United statesKisar stratfordCagefrom strykerUnivy osteovyMedtronic sofamor danekAscential ibd peekcDouble medical technologyShanghai sanyou medical coKj consulting corpMedacta internationalPioneer surgical technologyDrug administrationCranial guidance softwareMedos internationalSpine truss systemVertebral body replacement device

VySpine receives FDA 510(k) clearance of intervertebral body fusion system

VySpine has announced FDA 510(k) clearance of its UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion system, according to a press release.The UniVy OsteoVy-Ti NanoVy-HA cervical intervertebral body fusion (IBF) system is indicated for patients with degenerative disc disease who undergo IBF at one level in the cervical spine. According to the release, the system is designed with a

Gina brockenbroughUnivy osteovyUnivy osteovy ti

6 recent spine devices earning FDA nods

Here are six spine technologies earning FDA greenlights since March 1:

Implanet squaleUnivy osteovySolutions based spine platformOrthopedic technologiesSolutions based spineUnivy osteovy ti

VySpine s cervical IBF system earns FDA nod

VySpine s UniVy OsteoVy-Ti NanoVy-HA cervical IBF system earned FDA 510(k) clearance.

Vyspine univy osteovyUnivy osteovyUnivy osteovy ti

VySpine Announces FDA Clearance for UniVy OsteoVy-Ti Cervical IBF with NanoVy-HA

VySpine Announces FDA Clearance for UniVy OsteoVy-Ti Cervical IBF with NanoVy-HA
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