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Latest Breaking News On - Da 510k clearance - Page 1 : vimarsana.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
Rtificial-intelligence
Pp
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
Acroiliac-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
Nterior
Ransforaminal
Posterior
Orthofix launches new bioactive synthetic graft
Orthofix earned FDA 510(k) clearance for its OsteoCove advance bioactive synthetic graft, the company said Oct. 12.
Tyler-lipschultz
Orthofix
Da-510k-clearance
Steocove
Ioactive-synthetic-graft
Dputty
Trip-configurations
Hydroxyapatite
Typei-bovine
DePuy Synthes' new spine system earns FDA clearance
DePuy Synthes, Johnson and Johnson's orthopedic company, earned FDA 510(k) clearance for the TriALTIS spine system.
Johnson-medtech
Depuy-synthes
Spine-system
Ohnson-amp-johnson
Rthopedic
Da-510k-clearance
Rialtis-spine-system
Osterior-thoracolumbar
Pedicle-screw-system
Nstruments
Enabling-technology
Washington Hospital Healthcare System debuts robotic knee replacement system
Washington Hospital Healthcare System recently debuted Think Surgical's TMINI miniature robotic system for total knee replacements.
Alexander-sah
Institute-for-joint-restoration
Washington-hospital-healthcare-system
Think-surgical
Joint-restoration
Robotic-system
Think-surgical
Mini
Iniature
Ireless-handpiece
Total-knee-replacements
Da-510k-clearance
PathKeeper Surgical debuts 3D optical navigation for spinal surgery in the US
PathKeeper Surgical's 3D optical navigation system has been used in its first commercial lumbar spinal fusion surgery in the U.S. The system eliminates radiatio
Chevy-chase
District-of-columbia
United-states
Washington
Tushar-patel
Pathkeeper-surgical
Washington-orthopaedics
Sports-medicine
3d-optical-navigation
Pathkeeper-surgical
Lumbar-spinal-fusion
Smith+Nephew's shoulder replacement system earns FDA clearance
Smith+Nephew's Aetos shoulder system earned FDA 510(k) clearance, the devicemaker said June 12.
Nephew-president
Global-orthopedics-brad-cannon
Smith-nephew
Aetos-shoulder-system
Da-510k-clearance
Anatomic
Reverse-shoulder-replacement
Aetos-meta-stem
Tability
One-preservation
Patient-anatomy
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