vimarsana.com

Fda 510k News Today : Breaking News, Live Updates & Top Stories | Vimarsana

Spinal Simplicity gets FDA nod for sacroiliac joint system

Spinal Simplicity s Liberty-SI Lateral implant system earned FDA 510(k) clearance, the devicemaker said Dec. 11.

Spinal simplicityIberty siAteral implantFda 510kSacroiliac jointAcroiliac disruptionsDegenerative sacroiliitis

FloSpine earns FDA clearance for KeyLift system

FloSpine earned FDA 510(k) clearance for its KeyLift expandable interlaminar stabilization system, according to a Nov. 1 news release.

Cheng lun sooLun sooFda 510kSpinal stenosisLess invasiveNterlaminar stabilizationIntervertebral discsCheng lun soo

Xēnix Medical s interbody fusion device gets FDA nod

Xēnix Medical earned FDA 510(k) clearance for its NeoWave interbody system, the devicemaker said Oct. 10.

Ryan phillipsXēnix medicalFda 510kSpinal fusionsRyan phillips

AI spine image analysis platform earns FDA clearance

Medical Metrics Spine Camp platform earned FDA 510(k) clearance, the medtech company said Sept. 19.

Medical metric spine campMedical metricsPine campFda 510kIsualization reportsClinical assessmentsClinical workflowsEgmental parametersLobal parameters

FloSpine achieves 1st 3D-printed cervical spine implantation

FloSpine has successfully implanted the first Ti-Largo 3D printed cervical cage in partnership with the Research Park at Florida Atlantic University. The device

Boca ratonUnited statesJohn afsharPalm beach fla neuroscience instituteResearch parkFlorida atlantic universitySouth florida hospitalPanama anterior cervical platePalm beachNeuroscience instituteI largo3d printedResearch parkFlorida atlantic universityBoca ratonFda 510k

vimarsana © 2020. All Rights Reserved.