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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 simplicity
Iberty si
Ateral implant
Fda 510k
Sacroiliac joint
Acroiliac disruptions
Degenerative 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 soo
Lun soo
Fda 510k
Spinal stenosis
Less invasive
Nterlaminar stabilization
Intervertebral discs
Cheng 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 phillips
Xēnix medical
Fda 510k
Spinal fusions
Ryan 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 camp
Medical metrics
Pine camp
Fda 510k
Isualization reports
Clinical assessments
Clinical workflows
Egmental parameters
Lobal 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 raton
United states
John afshar
Palm beach fla neuroscience institute
Research park
Florida atlantic university
South florida hospital
Panama anterior cervical plate
Palm beach
Neuroscience institute
I largo
3d printed
Research park
Florida atlantic university
Boca raton
Fda 510k
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