Logo Medical XPRT
Companies
Products
Services
Software
Training
Applications
Sign in
List your business

Advertising options
  1. Home
  2. News
  3. bone screws
Show results for
Products
Services

Companies

News
Articles
Downloads
Videos

Refine by
Date

  • Older

Bone Screws Articles & Analysis

18 news found

gammaCore Sapphire Non-Invasive Vagus Nerve Stimulator (nVNS) Receives Unique National Product Code Number by the Belgian Pharmaceutical Association

gammaCore Sapphire Non-Invasive Vagus Nerve Stimulator (nVNS) Receives Unique National Product Code Number by the Belgian Pharmaceutical Association

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another device at the same time (e.g., TENS Unit, muscle ...

ByelectroCore, Inc.


electroCore, Inc. Announces Distribution Agreement with Joerns Healthcare, LLC

electroCore, Inc. Announces Distribution Agreement with Joerns Healthcare, LLC

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another device at the same time (e.g., TENS Unit, muscle ...

ByelectroCore, Inc.


gammaCore Non-Invasive Vagus Nerve Stimulation (nVNS) Improves Neurobehavioral Outcomes in a Model of Traumatic Brain Injury

gammaCore Non-Invasive Vagus Nerve Stimulation (nVNS) Improves Neurobehavioral Outcomes in a Model of Traumatic Brain Injury

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another device at the same time (e.g., TENS Unit, muscle ...

ByelectroCore, Inc.


gammaCore (Non-Invasive Vagus Nerve Stimulation; nVNS) Reduces Symptoms of Acute Withdrawal in Patients with Opioid Use Disorder

gammaCore (Non-Invasive Vagus Nerve Stimulation; nVNS) Reduces Symptoms of Acute Withdrawal in Patients with Opioid Use Disorder

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another device at the same time (e.g., TENS Unit, muscle ...

ByelectroCore, Inc.


Empirical Spine Receives FDA Breakthrough Device Designation for the LimiFlex Device Targeting Degenerative Spondylolisthesis

Empirical Spine Receives FDA Breakthrough Device Designation for the LimiFlex Device Targeting Degenerative Spondylolisthesis

LimiFlex, new to the US Market, is an investigational device designed as an alternative to spinal fusion for patients receiving surgical decompression for grade 1 lumbar degenerative spondylolisthesis with spinal stenosis. LimiFlex does not involve any screws or bone grafts, which disrupt the natural motion between spine segments. ...

ByEmpirical Spine, Inc.


FDA Accepts & Closes Empirical Spine`s Limiflex PMA Module II as a Motion-Preserving Alternative to Lumbar Fusion

FDA Accepts & Closes Empirical Spine`s Limiflex PMA Module II as a Motion-Preserving Alternative to Lumbar Fusion

The LimiFlex DST mimics and augments the anatomic ligaments to create natural, balanced motion across the spine without the use of invasive screws, rods, and bone grafts. After completion of the neural decompression/laminectomy, LimiFlex is implanted through the same incision to restore stability while maintaining balanced mobility of the spine. ...

ByEmpirical Spine, Inc.


electroCore, Inc. Announces Study of gammaCore Sapphire for the Treatment of Post-COVID Syndrome

electroCore, Inc. Announces Study of gammaCore Sapphire for the Treatment of Post-COVID Syndrome

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another device at the same time (e.g., TENS Unit, muscle ...

ByelectroCore, Inc.


electroCore, Inc. Announces gammaCore Non-Invasive Vagus Nerve Stimulator Available Through National Spine and Pain Centers

electroCore, Inc. Announces gammaCore Non-Invasive Vagus Nerve Stimulator Available Through National Spine and Pain Centers

gammaCore is contraindicated for patients if they: Have an active implantable medical device, such as a pacemaker, hearing aid implant, or any implanted electronic device Have a metallic device, such as a stent, bone plate, or bone screw, implanted at or near the neck Are using another device at the same time (e.g., TENS Unit, muscle ...

ByelectroCore, Inc.


Empirical Spine Submits PMA Module II for Limiflex as a New Motion-Preserving, Minimally Invasive Standard in Spine Surgery

Empirical Spine Submits PMA Module II for Limiflex as a New Motion-Preserving, Minimally Invasive Standard in Spine Surgery

It is compatible with current decompression techniques and is inserted without screws to reduce procedural morbidity and preserve the option for other treatments if needed. ...

ByEmpirical Spine, Inc.


Empirical Spine Advances LimiFlex as a New Motion-Preserving, Minimally Invasive Standard in Spine Surgery

Empirical Spine Advances LimiFlex as a New Motion-Preserving, Minimally Invasive Standard in Spine Surgery

LimiFlex can be performed in an outpatient setting, typically in less than 20 minutes. LimiFlex does not involve any screws or bone grafts, which can cause issues by eliminating the natural motion between spine segments. ...

ByEmpirical Spine, Inc.


Empirical Spine Presents Data from Study of the LimiFlex Tension Band at the Society for Minimally Invasive Spine Surgery (SMISS) Annual Forum 2021

Empirical Spine Presents Data from Study of the LimiFlex Tension Band at the Society for Minimally Invasive Spine Surgery (SMISS) Annual Forum 2021

” About LimiFlex The LimiFlex Tension Band is a new, investigational device designed as an alternative to spinal fusion for patients receiving surgical decompression for grade 1 lumbar degenerative spondylolisthesis with spinal stenosis. LimiFlex does not involve any screws or bone grafts, which eliminate the natural motion between spine segments. ...

ByEmpirical Spine, Inc.


Silver Bullet Therapeutics Secures CE Mark Approval for Revolutionary New Antimicrobial Bone Screw System

Silver Bullet Therapeutics Secures CE Mark Approval for Revolutionary New Antimicrobial Bone Screw System

Over the next few months, Silver Bullet will be finalizing launch plans with its prospective partners for selected European markets. The OrthoFuzIon Orthopedic Bone Screw System is the world’s first regulatory-approved antimicrobial bone screw product for orthopedic procedures. The OrthoFuzIon System expands upon the ...

BySilver Bullet Therapeutics, Inc.


Silver Bullet Therapeutics Reports Results of OrthoFuzIon Antimicrobial Bone Screw Testing Against the Top Six CDC Antibiotic Resistant “Superbugs”

Silver Bullet Therapeutics Reports Results of OrthoFuzIon Antimicrobial Bone Screw Testing Against the Top Six CDC Antibiotic Resistant “Superbugs”

Silver Bullet Therapeutics, Inc., a privately held medical device company that has developed an antimicrobial technology for implantable medical devices such as orthopedic bone screws, reported today the results of a study testing the “Time Kill” and “Adherence” effectiveness of its CE-marked OrthoFuzIon® Antimicrobial ...

BySilver Bullet Therapeutics, Inc.


Silver Bullet Therapeutics Announces Allowance of Patent # 9,248,254

Silver Bullet Therapeutics Announces Allowance of Patent # 9,248,254

Patent and Trademark Office allowed a new patent, BONE IMPLANTS FOR THE TREATMENT OF INFECTION. The company also announced that it has made an expedited CE Mark filing for a significantly expanded OrthoFuzIon Antimicrobial Bone Screw System product line. ...

BySilver Bullet Therapeutics, Inc.


Silver Bullet Therapeutics Announces Allowance of Two New Patents and Commercial Availability of the OrthoFuzIon Antimicrobial Bone Screw System

Silver Bullet Therapeutics Announces Allowance of Two New Patents and Commercial Availability of the OrthoFuzIon Antimicrobial Bone Screw System

Patent and Trademark Office allowed two new patents that include, COATINGS FOR THE CONTROLLABLE RELEASE OF ANTIMICROBIAL METAL IONS and BONE IMPLANT AND SYSTEMS THAT CONTROLLABLY RELEASES SILVER. The Company also announced that they will make the OrthoFuzIon Antimicrobial Bone Screw System commercially available to select institutions beginning ...

BySilver Bullet Therapeutics, Inc.


Silver Bullet Therapeutics Announces Issuance of U.S. Patent No. 8,999,367 for Bioabsorbable Substrates That Controllably Release Metal Ions

Silver Bullet Therapeutics Announces Issuance of U.S. Patent No. 8,999,367 for Bioabsorbable Substrates That Controllably Release Metal Ions

This uniquely allows us to protect the broad range of our antimicrobial devices from orthopedic screws, hip and knee prostheses and cardiac implantable defibrillators and pacemakers to venous access indwelling catheters, sutures, surgical mesh and even surgical ...

BySilver Bullet Therapeutics, Inc.


Silver Bullet Therapeutics Announces CE Mark Approval for the OrthoFuzIon Cannulated Bone Screw System

Silver Bullet Therapeutics Announces CE Mark Approval for the OrthoFuzIon Cannulated Bone Screw System

The OrthoFuzIon System consists of a platinum plated cannulated titanium bone screw and silver plated nitinol insert that fits into the inner lumen of the screw cannula. Implanted in the same manner as traditional bone screws and positioned to reduce and fixate a lower extremity fracture, the OrthoFuzIon ...

BySilver Bullet Therapeutics, Inc.


ASTM F1541 - 02(2011) standard specification and test methods for external skeletal fixation devices

ASTM F1541 - 02(2011) standard specification and test methods for external skeletal fixation devices

A7.1.1 This test method covers procedures for determining the stiffness, strength, and repetitive loading performance characteristics of external skeletal fixator-bone constructs when subjected to force loading (axial, medial-lateral shear, anterior-posterior shear) and moment loading (torsion, medial-lateral bending, anterior-posterior bending). ...

ByASTM International

  • Previous
  • Next
Need help finding the right suppliers?Try XPRT Sourcing. Let the XPRTs do the work for you
Back to top
About Medical XPRT

Medical XPRT is a global marketplace with solutions and suppliers for the medical sector, with product catalogs, articles, industry events, publications & more.

Channels

Solutions

  • Medical XPRT Industry Products
  • Medical XPRT Industry Software
  • Medical XPRT Industry Training
  • Medical XPRT Industry Services
  • Medical XPRT Industry Applications

Latest

  • Medical XPRT Industry News
  • Medical XPRT Industry Events

Publications

  • Medical XPRT Industry Articles
  • Medical XPRT Industry Books
  • Medical XPRT Industry Magazines
  • Medical XPRT Industry Downloads
  • Medical XPRT Industry Videos

Companies

  • Medical XPRT Industry Companies

  • FAQs
  • Company sitemap
  • Category sitemap
Medical XPRT is part of XPRT Media All Rights Reserved.
Terms
Privacy
  • Medical XPRT RSS List
Our sites:
Environmental XPRT
Agriculture XPRT
Energy XPRT
XPRT