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LimaCorporate, TechMah Medical get FDA approval for 3D shoulder planning system
LimaCorporate and TechMah Medical received FDA 510(k) approval for the Smart Space Shoulder 3D Planner & 3D Positioner Dec. 9. - 12/9/19 -
2 recent orthopedic device company acquisitions — November
Here are two orthopedic company transactions in the past month. - 12/9/19 -
DePuy Synthes recalls devices used in spine fixation system: 6 things to know
Johnson & Johnson's DePuy Synthes is voluntarily recalling its USS II Polyaxial 3D heads, according to an urgent field safety notice issued out of Switzerland Nov. 11. - 12/6/19
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Ulrich Medical USA launches 1st rod-screw system for spine surgery
Ulrich Medical USA launched its debut rod-screw system for spine surgery on Dec. 6 - 12/6/19 -
Mainstay Medical receives Australian approval for neurostimulation implant
The Australian Therapeutic Goods Administration provided regulatory approval for Mainstay Medical's ReActiv8 system. - 12/6/19 -
DePuy Synthes unveils new system for cervical, thoracic spine surgery
DePuy Synthes launched its Symphony Occipito-Cervico-Thoracic System Dec. 6, expanding its portfolio for the treatment of cervical and thoracic spine disorders, reports News Medical Life Sciences. - 12/6/19 -
Hensler Surgical alleges patent infringement after Tobra CEO inquired about becoming a sales rep: 4 details
Hensler Surgical Technologies filed a lawsuit against Tobra Medical over patent infringement. - 12/6/19
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Empirical Spine finishes enrollment for implant in degenerative spondylolisthesis clinical trial
The investigational arm of Empirical Spine's IDE clinical trial completed enrollment Dec. 4 for its study of the LimiFlex Paraspinous Tension Band. - 12/5/19 -
Meet the new president of Orthofix's global spine business: Kevin Kenny
Orthofix Medical named Kevin Kenny, formerly Medtronic Spine and Biologics' vice president of U.S. sales, its new president of global spine Dec. 5. - 12/5/19 -
Former device company CEO charged with fraud & more: 7 device company key notes
Here are seven key notes on spine and orthopedic device companies: - 12/4/19 -
Johnson & Johnson subsidiary launches product for surgical bleeding: 5 things to know
Johnson & Johnson subsidiary Ethicon debuted its Vistaseal Fibrin Sealant, a product designed to help surgeons manage intraoperative bleeding. - 12/4/19
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Stanford to acquire 2nd CyberKnife M6 system for neurosurgery
Palo Alto, Calif.-based Stanford University Medical Center is expanding access to neurosurgery treatments by acquiring a second CyberKnife M6 system. - 12/4/19 -
SPR Therapeutics reports completion of 1,000th nerve stimulation procedure for OA
SPR Therapeutics announced the commercial placement of its 1,000th Sprint Peripheral Nerve Stimulation system for pain was completed Dec. 4. - 12/4/19 -
Medtronic, Lumeon partner for value-based care platform in Europe
Medtronic and Lumeon entered into a strategic partnership that aims to help healthcare providers in Europe succeed with value-based care. - 12/4/19 -
RTI Surgical shakes up leadership team, adds former Alphatec CEO — 4 insights
RTI Surgical Holdings made a pair of appointments to its leadership team, as the company works to redefine its image as a spine and original equipment manufacturer. - 12/3/19 -
Vertos Medical concludes enrollment of study for lumbar spinal stenosis procedure
Vertos Medical completed the enrollment of its nationwide study of its Mild procedure for lumbar spinal stenosis on Dec. 3. - 12/3/19 -
Smith+Nephew discloses completion of 1st procedures with new knee device
The first procedures with Smith+Nephew's Journey II Unicompartmental Knee System were reported Dec. 3. - 12/3/19 -
RTI Surgical receives FDA clearance for spinal fixation device
RTI Surgical received FDA 510(k) clearance for its Streamline MIS Spinal Fixation System on Dec. 2, reports Seeking Alpha. - 12/2/19 -
Spinal fusion devices market to hit $8.45B by 2026 — 4 takeaways
The spinal fusion devices market is expected to reach $8.45 billion by 2026, according to a market report by Fortune Business Insights. - 12/2/19 -
North Carolina patient sues Medtronic over failed spinal fusion
Medtronic is being sued by a man from North Carolina after an implanted pedicle screw allegedly broke and caused him to undergo revision surgery, reports The Times News. - 12/2/19