ZygoFix Receives FDA Clearance for its zLOCK Lumbar Facet Fixation System
MISGAV,
Spinal fusion, a common surgical procedure performed for degenerative spinal conditions such as Spondylolisthesis, Spinal Stenosis, and degenerative disc disease, traditionally requires placement of 4 screws and 2 rods, creating an artificial bridge, to stabilize the segment. The conventional invasive approach requires precise placement and building of bridges intraoperatively. ZygoFix's revolutionary zLOCK system harnesses the spine's innate bone structure to securely lock its connecting joints. Unlike traditional methods, the company's innovative implant adapts to the joint's anatomy during insertion, offering unparalleled stability with a minimally invasive, simple procedure that can be performed in outpatient and ASC environments.
With CE certification and six years of clinical utilization yielding long-term pain reduction and bone growth, ZygoFix's zLOCK Lumbar Facet Fixation System is positioned to revolutionize spinal fusion surgery.
ZygoFix CEO
Dr. Nicholas Pachuda, ZygoFix Chair, added: "Obtaining 510(k) clearance is a testament to ZygoFix's commitment to innovation and addressing the unmet needs of patients suffering from degenerative spinal conditions. We eagerly anticipate offering patients our minimally invasive, life-changing solution in
Dr.
About ZygoFix
ZygoFix Ltd. is a spine device company, a portfolio company of the Trendlines Group (SGX: 42T) (OTCQX: TRNLY), and has been supported by the Israel Innovation Authority and the European EIC program, alongside The Trendlnes Group and investors worldwide. The Company's inventions enable internal joint stabilization while conforming to the joint's anatomy.
Contact Information
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View original content:https://www.prnewswire.com/news-releases/zygofix-receives-fda-clearance-for-its-zlock-lumbar-facet-fixation-system-302136657.html
SOURCE ZygoFix
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