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Orthopedic Devices News

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31-45 of 1566 results
OIC introduces Intramedullary Tibial Nailing system
Medical device firm The Orthopaedic Implant Company (OIC) has introduced Intramedullary Tibial Nailing system to stabilize fractures of the tibia.
Specialty Devices > Orthopedic Devices > News
Camber Spine gets FDA approval for Siconus SI joint fixation system
By MDBR Staff Writer
Musculoskeletal implant firm Camber Spine Technologies has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its Siconus SI joint fixation system.
Specialty Devices > Orthopedic Devices > News
The NBA, GE Healthcare issue call for proposals to address bone stress injuries
The National Basketball Association (NBA) & GE Healthcare Orthopedics and Sports Medicine Collaboration issued a new call for proposals (CFP) focused on bone stress injuries (BSI), a frequent and debilitating injury for both the elite and the everyday athlete.
Specialty Devices > Orthopedic Devices > News
Ossdsign Cranial patient-specific medical implant wins FDA 510(k) clearance
By MDBR Staff Writer
Sweden-based OssDsign has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its Ossdsign Cranial PSI to market in the country.
Specialty Devices > Orthopedic Devices > News
Precision Spine wins FDA 510(k) clearance for ShurFit ACIF 2C anterior cervical interbody system
By MDBR Staff Writer
Medical device firm Precision Spine has secured 510(k) clearance for its ShurFit ACIF 2C anterior cervical interbody system.
Specialty Devices > Orthopedic Devices > News
Spinal Elements reveals results of Magnum+ ALIF device’s retrospective study
Spinal Elements, a spine technology company, announced the publication of data obtained from a retrospective study involving the use of the company’s Magnum+ device used in anterior lumbar interbody fusion (ALIF).
Specialty Devices > Orthopedic Devices > News
FDA approves CyMedica’s app-controlled muscle activation therapy
By MDBR Staff Writer
CyMedica Orthopedics has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its e-vive app-controlled and data-driven muscle activation therapy and patient engagement solution.
Specialty Devices > Orthopedic Devices > News
FDA approves SpineGuard's DSG integration module to make pedicle screws smart
By MDBR Staff Writer
SpineGuard has secured approval from the US Food and Drug Administration (FDA) for its new DSG (dynamic surgical guidance) integration module for making pedicle screws smart.
Specialty Devices > Orthopedic Devices > News
Safe Orthopaedics launches Walnut cervical cage bone substitute in Europe
By MDBR Staff Writer
French medical technology Safe Orthopaedics has introduced a bone substitute for its Walnut cervical cage in Europe.
Specialty Devices > Orthopedic Devices > News
Orthocell announces collaboration with Johnson & Johnson Innovation
Regenerative medicine company Orthocell has announced a research collaboration agreement with DePuy Synthes Products, part of the Johnson & Johnson Family of Companies, for its Ortho-ATI stem cell approach for the regeneration of degenerate tendons and ligaments.
Specialty Devices > Orthopedic Devices > News
Osseon receives new patent for steerable and curvable cavity creation system
Osseon has received a new patent for a steerable and curvable cavity creation system, with number US 9,510,885.
Specialty Devices > Orthopedic Devices > News
Medovex signs international distribution agreement with AlfaMed
Medovex, a developer of medical technology products, has entered into an international distribution agreement with AlfaMed, a supplier of innovative spine surgery equipment.
Specialty Devices > Orthopedic Devices > News
Medicrea announces 510(k) submission for FDA clearance of 3D-printed titanium spinal interbody devices
The Medicrea Group has announced the filing of its 510(k) submission to the US Food and Drug Administration (FDA) for approval of the company’s 3D-printed Titanium interbody devices, with compatible UNiD Lab personalized surgical planning and analytical services.
Specialty Devices > Orthopedic Devices > News
AVEX raises $7.6m in series A financing round to support launch of Footbeat
AVEX announced the securing of $7.6m in series A financing that will fuel the Q1 2017 launch of Footbeat.
Specialty Devices > Orthopedic Devices > News
Johnson & Johnson Medical Devices Companies introduce Orthopaedic Episode of Care Approach
The Johnson & Johnson Medical Devices Companies announced their Orthopaedic Episode of Care Approach, a comprehensive offering under their CareAdvantage capabilities, designed to help health systems and surgeons reduce costs and increase quality to drive improvements in orthopaedic care and achieve the goals of value-based alternative care models.
Specialty Devices > Orthopedic Devices > News
31-45 of 1566 results