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1-15 of 1865 results
FDA approves expanded indication for NuVasive’s TLX interbody system
By MDBR Staff Writer
The US Food and Drug Administration (FDA) has approved an expanded indication for NuVasive’s TLX interbody system to use in spinal fusion surgery.
Specialty Devices > Orthopedic Devices > News
DePuy Synthes launches 3D simulation assisted Maxframe multi-axial correction system
By MDBR Staff Writer
Johnson & Johnson (J&J) business unit DePuy Synthes has introduced new 3D simulation assisted orthopaedic external circular fixation device to treat patients with limb deformity.
Specialty Devices > Orthopedic Devices > News
ManaMed launches deep vein thrombosis prevention device PlasmaFlow
By MDBR Staff Writer
California-based ManaMed has launched the US Food and Drug Administration (FDA) approved deep vein thrombosis (DVT) prevention device – PlasmaFlow – in the US.
Specialty Devices > Orthopedic Devices > News
Logiciel de contrôle et supervision pour installations de stérilisation à l’EtO
Fabricant d'équipements de stérilisation à l'oxyde d'éthylène (EtO), STERISYS a développé son propre logiciel de supervision conformément aux directives GAMP 5 et FDA 21 CFR Part 11. Celui-ci permet de contrôler l'ensemble d'une installation à partir d'une seule IHM.
Specialty Devices > Orthopedic Devices > Press Releases
K2M launches Everest minimally invasive XTower instrumentation
K2M Group Holdings has launched Everest minimally invasive (MI) XTower instrumentation, an enhancement to the Everest MI XT spinal system, at the Society for Minimally Invasive Spine Surgery Annual Forum (SMISS) event.
Specialty Devices > Orthopedic Devices > News
Spinal Resources’ Swedge pedicle screw system gets FDA 510(k) clearance
Spinal Resources (SRI) announced that it has received FDA 510(k) clearance for its Swedge pedicle screw system.
Specialty Devices > Orthopedic Devices > News
Bioness to showcase lower extremity product portfolio at American Orthotic & Prosthetic Association World Congress
Bioness will showcase its lower extremity product portfolio at the centennial American Orthotic and Prosthetic Association (AOPA) World Congress, September 6th-9th in Las Vegas, Nevada.
Specialty Devices > Orthopedic Devices > News
FDA approves NuVasive’s redesigned Magec system
By MDBR Staff Writer
Medical devices maker NuVasive has secured 510(k) clearance from the US Food and Drug Administration (FDA for its redesigned Magec system to be used with Reline small stature system.
Specialty Devices > Orthopedic Devices > News

MDBR Supplier Recommendations

STERISYS - Your Solution and Service Provider for Industrial Sterilisation
STERISYS is the European leader in industrial EO sterilisation and offers a wide range of solutions to medical device manufacturers and sterilisation service providers.... Specialty Devices > Orthopedic Devices > Suppliers
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1-15 of 1865 results