US2006173545A1PendingUtilityA1
Spinal disc annulus reconstruction method and deformable spinal disc annulus stent
Est. expiryOct 20, 2019(expired)· nominal 20-yr term from priority
Inventors:Joseph CauthenMatthew M. BurnsLawrence W. WalesBrian L. DukartBradley J. WessmanRodney L. Houfburg
A61F 2002/30092A61F 2002/30062A61F 2002/30579A61F 2210/0019A61F 2/442A61F 2002/2817A61F 2002/30158A61F 2/30907A61B 17/06166A61F 2002/30777A61F 2/0063A61F 2002/4435A61F 2002/30784A61F 2002/4627A61F 2/4611A61B 2017/06176A61B 17/0642A61F 2310/00011A61F 2230/0093A61B 2017/0641A61F 2230/0026A61F 2002/30299A61B 17/86A61B 2017/0648A61F 2/4601A61F 2002/30841A61B 17/04A61F 2210/0004A61F 2002/444A61B 2017/00004A61B 2017/0647A61F 2/441
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Claims
Abstract
A spinal disc annulus repair stent for repair and reconstruction of the spinal disc wall (annulus) after surgical invasion or pathologic rupture, which may incorporate suture closure or other means of stent insertion and fixation, designed to reduce the failure rate of conventional surgical procedures on the spinal discs. In an illustrative embodiment, the design of the spinal disc annulus stent advantageously allows ingrowth of normal cells of healing in an enhanced fashion strengthening the normal reparative process.
Claims
exact text as granted — not AI-modified1 . A device for treating an aperture in the annulus of a patient's intervertebral disc, said device comprising a cylindrical body formed of a plurality of filamentous elements, said body having a radial diameter, a first end and a second end subtending a longitudinal dimension, said device having a first configuration, and a second configuration, wherein the second configuration, in use, is characterized by a relatively larger radial diameter along at least a portion of said longitudinal dimension.
2 . The device of claim 1 , wherein said body is sized to be inserted through said aperture in a intervertebral disc into the subannular space in said first configuration and then placed in said second configuration to at least partially cover said aperture.
3 . The device of claim 1 , wherein said second configuration is additionally characterized by a relatively smaller longitudinal dimension in said second configuration than in said first configuration.
4 . The device of claim 1 , wherein at least a portion of the stent is formed at least in part of flexible biocompatible material.
5 . The device of claim 1 , wherein at least a portion of the stent is formed at least in part of bioresorbable material.
6 . The device of claim 1 , wherein at least a portion of the stent is formed at least in part of nylon.
7 . The device of claim 1 , wherein at least a portion of the stent is formed at least in part by weaving.
8 . The device of claim 1 , wherein at least a portion of the stent is formed at least in part by braiding.Cited by (0)
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