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Limiflex Dynamic Sagittal Tether
Details
Device typeLumbar decompression interspinous spacer: A device intended to be implanted between two adjacent lumbar spinous processes during a minimally-invasive procedure to decompress neural structures, typically to treat a patient with symptomatic degenerative lumbar spinal stenosis (DLSS). It is typically designed as a small spacer, either a single-piece or assembly, made of metal [e.g., titanium (Ti), nickel-titanium alloy (Nitinol)] and/or synthetic polymer [e.g., hydrogel, polyetheretherketone (PEEK)]. Disposable devices associated with implantation (e.g., introducer needles, trocars) may be included with the device.
FDA categoryProsthesis, Spinous Process Tension Band Implant
Device ID00859373004005
Catalog numberKLF-3001
AvailabilityPrescription
Single useYes
SterileYes
MRI safetyMR Conditional