Medtronic has received FDA 510(k) clearance and breakthrough device designation for its LigaPass 2.0 ligament augmentation system.
Spinal Tech
The FDA gave an investigational device exemption to spine devicemaker 3Spine.
SeaSpine released its WaveForm C interbody system in a full commercial launch.
A devicemaker's spine surgery milestone and four more updates from medtech companies in the last week:
Inspired Spine reached more than 1,500 oblique lateral lumbar interbody spinal fusion procedures.
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Knoxville, Tenn.-based ChoiceSpine is partnering with France-based eCential Robotics to combine their technologies into one system.
From a spine-specific operating table to new navigation systems, here is what to know about five technologies that have recently debuted and cleared or approved by the FDA.
Medical device company Sure Retractors will showcase its new cervical and mini-open retractor during the Becker's Healthcare 19th annual Spine, Orthopedic and Pain Management-Driven ASC Conference June 16-18.
VisAR, an augmented reality surgical guidance system, received FDA approval for intraoperative spine surgery.
SeaSpine's latest device launch and five more updates from spine medtech companies in the last week: