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Latest Breaking News On - Da 510k clearance - Page 1 : comparemela.com
Nevro earns FDA clearance for SI joint fixation system
Nevro earned FDA 510(k) clearance to use its sacroiliac joint fixation system without having to include a lateral screw, the devicemaker said Feb. 28.
Kevin-thornal
Vyrsa-technologies
Meta-keywords-nevro
Da-510k-clearance
Acroiliac-joint-fixation-system
Ateral-screw
Devicemaker
Transfix
Ong-term-fusion
Self-contained
Deployable
Medtech news ASC leaders should know
Discover the latest developments in medtech, including FDA approvals, new appointments, and partnerships that ASC leaders should know about.
Raman-venkatesh
Zimmer-biomet
Medtronic
Waldemar-link-gmbh-co
Momentum-health
Momentum-spine
Bone-ortho
Waldemar-link-gmbh
Medtech
Asc-leaders
Zimmer-biomet
Fda-clearance
Momentum Health earns FDA approval for AI spine app
Momentum Health earned FDA 510(k) clearance for Momentum Spine, an artificial intelligence-powered app for spine care.
Canada
Health-canada
Momentum-health
Momentum-spine
Meta-keywords-momentum-health
Da-510k-clearance
Momentum-spine
Artificial-intelligence
App
Spine-care
Ostural-asymmetries
SI-Bone gets clearance for smaller version of spine implant
SI-Bone earned FDA 510(k) clearance of the iFuse Bedrock Granite implant system in a smaller diameter, according to a Jan. 30 news release.
Technology-payment
Fuse-bedrock-granite
Breakthrough-device-designation
New-technology-add-on-payment
Si-bone
Da-510k-clearance
Maller-diameter
Expanded-indication
Pediatric-patients
1-trajectory
Sacroiliac-fusion
Curiteva gets FDA clearance for Inspire lumbar interbody system
Curiteva s Inspired 3D-printed lumbar interbody fusion system earned FDA 510(k) clearance, the devicemaker said Jan. 22.
Fused-filament-fabrication
Inspire-trabecular
Meta-keywords-curiteva
Nspired
3d-printed
Lumbar-interbody-fusion-system
Da-510k-clearance
Devicemaker
Interior
Ransforaminal
Posterior
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