Patent Application
20220031469
The present disclosure relates generally to medical devices, and more specifically it relates to intervertebral and intradiscal devices, systems, and methods for deployment within a body of a patient.
In mammals, the spinal (or vertebral) column is one of the most important parts. The spinal column provides the main support necessary for mammals to stand, bend, and twist.
In humans, the spinal column is generally formed by individual interlocking vertebrae, which are classified into five segments, including (from head to tail) a cervical segment (vertebrae C1-C7), a thoracic segment (vertebrae T1-T12), a lumbar segment (vertebrae L1-L5), a sacrum segment (vertebrae S1-S5), and coccyx segment (vertebrate Co1-Co5). The cervical segment forms the neck, supports the head and neck, and allows for nodding, shaking and other movements of the head. The thoracic segment attaches to ribs to form the ribcage. The lumbar segment carries most of the weight of the upper body and provides a stable center of gravity during movement. The sacrum and coccyx make up the back walls of the pelvis.
Intervertebral discs are located between each of the movable vertebra. Each intervertebral disc typically includes a thick outer layer called the disc annulus, which includes a crisscrossing fibrous structure, and a disc nucleus, which is a soft gel-like structure located at the center of the disc. The intervertebral discs function to absorb force and allow for pivotal movement of adjacent vertebra with respect to each other.
In the vertebral column, the vertebrae increase in size as they progress from the cervical segment to the sacrum segment, becoming smaller in the coccyx. At maturity, the five sacral vertebrae typically fuse into one large bone, the sacrum, with no intervertebral discs. The last three to five coccygeal vertebrae (typically four) form the coccyx (or tailbone). Like the sacrum, the coccyx does not have any intervertebral discs.
Each vertebra is an irregular bone that varies in size according to its placement in the spinal column, spinal loading, posture and pathology. While the basic configuration of vertebrae varies, every vertebra has a body that consists of a large anterior middle portion called the centrum and a posterior vertebral arch called the neural arch. The upper and lower surfaces of the vertebra body give attachment to intervertebral discs. The posterior part of a vertebra forms a vertebral arch that typically consists of two pedicles, two laminae, and seven processes. The laminae give attachment to the ligament flava, and the pedicles have a shape that forms vertebral notches to form the intervertebral foramina when the vertebrae articulate. The foramina are the entry and exit passageways for spinal nerves. The body of the vertebra and the vertical arch form the vertebral foramen, which is a large, central opening that accommodates the spinal canal that encloses and protects the spinal cord.
The body of each vertebra is composed of cancellous bone that is covered by a thin coating of cortical bone. The cancellous bone is a spongy type of osseous tissue, and the cortical bone is a hard and dense type of osseous tissue. The vertebral arch and processes have thicker coverings of cortical bone.
The upper and lower surfaces of the vertebra body are flattened and rough. These surfaces are the vertebral endplates that are in direct contact with the intervertebral discs. The endplates are formed from a thickened layer of cancellous bone, with the top layer being denser. The endplates contain adjacent discs and evenly spread applied loads. The endplates also provide anchorage for the collagen fibers of the disc.
As noted earlier, each disc 6 comprises a fibrous exterior surrounding an inner gel-like center which cooperate to distribute pressure evenly across each disc 6, thereby preventing the development of stress concentrations that might otherwise damage and/or impair vertebrae 4 of spinal column 2. Discs 6 are, however, subject to various injuries and/or disorders which may interfere with a disc's ability to adequately distribute pressure and protect vertebrae 4. For example, disc herniation, degeneration, and infection of discs 6 may result in insufficient disc thickness and/or support to absorb and/or distribute forces imparted to spinal column 2. Disc degeneration, for example, may result when the inner gel-like center begins to dehydrate, which may result in a degenerated disc 8 having decreased thickness. This decreased thickness may limit the ability of degenerated disc 8 to absorb shock which, if left untreated, may result in pain and/or vertebral injury.
While pain medication, physical therapy, and other non-operative conditions may alleviate some symptoms, such interventions may not be sufficient for every patient. Accordingly, various procedures have been developed to surgically improve patient quality of life via abatement of pain and/or discomfort. Such procedures may include, discectomy and fusion procedures, such as, for example, anterior cervical interbody fusion (ACIF), anterior lumbar interbody fusion (ALIF), direct lateral interbody fusion (DLIF) (also known as XLIF), posterior lumbar interbody fusion (PLIF), and transforaminal lumbar interbody fusion (TLIF). During a discectomy, all or a portion of a damaged disc (for example, degenerated disc 8, shown in
Following the discectomy procedure, a medical professional may determine an appropriate size of an interbody device 10 (shown in
Often, following the removal of the distractor and/or trial, a medical professional must prepare one or more bores or holes in a vertebra intended to receive the bone screws. Such holes may be formed with the aid of a separate drill guide positioned proximate or abutting vertebra and inserting a drill therethrough. Alternatively, such holes may be formed free hand, without the use of a drill guide. Further, since the spinal column is subject to dynamic forces, often changing with each slight movement of the patient, such screw(s) have a tendency to back out (for example, unscrew) and/or dislodge from the interbody device, thereby limiting interbody device's ability to stabilize adjacent vertebrae, and consequently, promote fusion. Additionally, if the screw(s) back out and/or dislodge from the interbody device, they may inadvertently contact, damage, and/or irritate surrounding tissue. Further, the interbody device is commonly comprised of a radiopaque material so as to be visible in situ via x-ray and other similar imaging modalities. However, such materials may impede sagittal and/or coronal visibility, thereby preventing visual confirmation of placement and post-operative fusion.
Furthermore, while all metal titanium interbody devices may be generally good for bone ingrowth, they are radio-opaque and, thus, not good for monitoring bony fusion.
Thus, there remains a need for improved interbody devices, associated systems, and methodologies related thereto.
Accordingly, one aspect of the present disclosure provides a cage structure that can be made of different materials and textures. The cage structure may include various end surface textures with enhanced bone ingrowth while allowing for monitoring bony fusion.
According to an aspect of the present disclosure, an intervertebral cage structure is provided that comprises: a main body comprising a first surface and a second surface located opposite to the first surface; a plate disposed on the first surface of the main body; and an opening formed in the main body and extending from the first surface to the second surface located opposite the first surface, wherein the plate comprises a surface pattern having at least one of a symmetrical geometric pattern and an asymmetrical geometric pattern. The intervertebral cage structure may comprise a second plate disposed on the second surface of the main body. The main body may comprise a first material such as Polyether Ether Ketone (PEEK), Silicon Nitride (Si3N4) or other materials. The plate may comprise titanium or a titanium alloy.
The main body may further comprise a plurality of lateral surfaces extending between the first and second surfaces; and one or more holes extending from one of the plurality of lateral surfaces towards the opening. The main body may further comprise an inner surface surrounding the opening. The inner surface may comprise a bulged portion surrounding a portion of the one or more holes.
The intervertebral cage structure may comprise a pin hole extending from the plate to the main body, and a pin that inserts into the pin hole.
The main body may further comprise one or more slots, and the plate may comprise one or more tabs that insert into the plurality of slots of the main body to secure the first plate to the main body. The plate may comprise a cutout that renders the plate compressible.
In various embodiments, the intervertebral cage structure may comprise a plurality of different material, which may be assembled into a unitary implant body (i.e., a “hybrid” cage). In various embodiments, such a hybrid cage may comprise a shell main body, wherein the shell main body may be configured to receive and substantially encapsulate a central body. The shell main body may comprise a clam shape that includes said plate and the second plate, wherein said plate and the second plate are connected by a bridge portion. The main body may comprise at least one of a metal, PEEK, silicon, silicon nitride or other ceramic and/or allograft.
According to another aspect of the disclosure, an intervertebral cage structure is provided that comprises: a shell main body having a clam shape and comprising a bridge portion and wing portions extending from the bridge portion; first and second surface layers disposed on the first and second wing portions; and an opening formed in the main body and extending from the first surface layer to the second surface layer. At least one of the first surface layer and the second surface layer may comprise at least one of a symmetrical geometric pattern and an asymmetrical geometric pattern. The shell main body may comprise PEEK or Si3N4 and at least one of the first and second surface layers may comprise titanium or a titanium alloy.
The intervertebral cage structure may comprise an insertion section. The insertion section may be disposed between the first and second wing portions of the main body, wherein the opening may extend from the first surface layer to the second surface layer via the insertion section. The insertion section may comprise at least one of a metal, PEEK, Si3N4, silicon or allograft.
The intervertebral cage structure may comprise: a plurality of lateral surfaces extending between the first and second wing portions; and one or more holes extending from one of the plurality of lateral surfaces toward the opening.
The intervertebral cage structure may further comprise an inner surface surrounding the opening and having a bulged wall portion surrounding a portion of the one or more holes. In some embodiments, it may be desirous to include the bulged portion to provide an increased thickness of material to allow for longer threading, which may be helpful for securement to and/or anchoring of softer materials such as PEEK or relatively brittle materials such as Si3N4. In other embodiments, the bulge may be lessened and/or dispensed with, such as in titanium implant components, and/or a lesser number of threads or other securement components in a titanium material can accommodate the anticipated loading of the implant. Where such bulge can be removed or dispensed with, such a modification will desirably increase the overall size and/or cross-section of the bone graft window.
The intervertebral cage structure may include at least one slot and a guide that engages and guides the slot as the insertion section is installed in the shell main body.
The intervertebral cage structure may further comprise: a plurality of lateral surfaces; and one or more screw holes extending from one of the plurality of lateral surfaces to the opening.
The intervertebral cage structure and/or shell may further comprise first and second ears extending from the first and second wing portions, extending outwardly from each other, the first and second ears comprising one or more screw holes.
The implant may include surface patterns having multiple textures for immediate bonding or “Velcro” effect with surrounding tissues, such as bony surfaces, and/or the surface patterns may incorporate voids, undercuts and/or increased surface areas to desirably promote bony ingrowth and/or interdigitation. For example, the surface pattern of the intervertebral cage structure may comprise first and second protrusions adjacent each other with a gap therebetween, wherein the first and second protrusions have an undercut at a lower portion thereof, wherein superior surfaces of the first and second protrusions may have different shapes, and wherein at least one of the first and second protrusions may have a pocket formed at the bottom surface thereof.
According to a further aspect of the disclosure, an intervertebral cage structure is provided that comprises a surface configured to contact a vertebra, the surface comprising first and second protrusions adjacent each other with a gap formed therebetween, the first and second protrusions having an undercut formed at a lower portion thereof. The superior surfaces of the first and second protrusions have different shapes. At least one of the first and second protrusions may have a pocket formed on the surface thereof. If desired, the protrusions may be of the same of different heights, shapes and/or other geometries, and may be provided in a repeating pattern across a surface of the implant.
In various embodiments an intervertebral cage may comprise a shell main body, wherein the shell main body may be configured to receive and substantially encapsulate an inner main body. The shell main body may comprise a clam shape or similar construction that includes a first plate and a second plate, with a bridge extending therebetween and connecting the first and second plates. The main body may comprise at least one or a combination of metals, PEEK, silicon nitride and/or allograft.
According to another aspect of the disclosure, an intervertebral cage structure can be provided that comprises a shell main body having a clam-shape and comprising a bridge portion and wing portions extending from the bridge portion; first and second surface layers disposed on the first and second wing portions; and an opening formed in the main body and extending from the first surface layer to the second surface layer. At least one of the first surface layer and the second surface layer may comprise at least one of a symmetrical geometric pattern and an asymmetric geometric pattern. The shell main body may comprise PEEK or silicon nitride (or a combination thereof) and at least one of the first and second surface layers may comprise titanium and/or a titanium alloy.
The intervertebral cage may comprise an insertion body, with the insertion body disposed between the first and second wing portions of the main body, wherein the opening may extend from the first surface layer to the second surface layers via the insertion body. The insertion body may comprise one or more of the following: a metal, PEEK, silicon nitride and/or an allograft.
In accordance with various aspects of the present subject matter, implant devices and/or components thereof are described that incorporate silicon nitride (i.e., Si3N4 and/or chemical analogues thereof) in their construction, either in the entirety of the implant as well as components, portions, layers and/or surfaces thereof. In various embodiments, the silicon nitride material(s) will be highly osteo-inductive and/or osteoconductive and will desirably facilitate and/or promote implant fixation to adjacent living bone surfaces, while concurrently reducing and/or inhibiting periprosthetic infection and/or bacterial adhesion to the surfaces and/or interior portions of the implant.
In various applications, the utility of silicon nitride as an implant material can be enhanced by the addition of various other medical materials, including the use of one or various combinations of titanium, chrome cobalt, stainless steel, silicone, poly (ether ketone) (PEEK), ultra-high molecular-weight polyethylene (UHMWPE), polyurethane foams, polylactic acid, apatites and/or various 3D printed materials. In such cases, the employment of such material mixtures in implant construction may enhance the strength and/or durability of a desired implant design, as well as allow for improved surgical outcomes and/or greatly reduced complication rates.
If desired, implants can be constructed from a variety of modular components, including modular components comprising different materials. If desired, such modular components could be provided in a kit form for selection and/or assembly in a surgical theatre and/or in situ during a surgical procedure. If desired, various components may be removable and replaceable.
In various embodiments, a surface pattern of the intervertebral cage may comprise first and second protrusions adjacent to each other with a gap therebetween, wherein one or both of the first and second protrusions include an undercut portion at a lower portion thereof, wherein superior surfaces of the first and/or second protrusions may have the same or differing shapes, and wherein at least one of the first and second protrusions may have a pocket formed at the bottom surface thereof.
Additional features, advantages, and embodiments of the disclosure may be set forth or apparent from consideration of the following detailed description, drawings, and claims. Moreover, it is to be understood that both the foregoing summary of the disclosure and the following detailed description are exemplary and intended to provide further explanation without limiting the scope of the disclosure as claimed.
The accompanying drawings, which are included to provide a further understanding of the disclosure, are incorporated in and constitute a part of this specification, illustrate embodiments of the disclosure and together with the detailed description serve to explain the principles of the disclosure. No attempt is made to show structural details of the disclosure in more detail than may be necessary for a fundamental understanding of the disclosure and the various ways in which it may be practiced. In the drawings:
The disclosure and the various features and advantageous details thereof are explained more fully with reference to the non-limiting embodiments and examples that are described and/or illustrated in the accompanying drawings and detailed in the following description. It should be noted that the features illustrated in the drawings are not necessarily drawn to scale, and features of one embodiment may be employed with other embodiments as the skilled artisan would recognize, even if not explicitly stated herein. Descriptions of well-known components and processing techniques may be omitted so as to not unnecessarily obscure the embodiments of the disclosure. The examples used herein are intended merely to facilitate an understanding of ways in which the disclosure may be practiced and to further enable those of skill in the art to practice the embodiments of the disclosure. Accordingly, the examples and embodiments herein should not be construed as limiting the scope of the disclosure. Moreover, it is noted that like reference numerals represent similar parts throughout the several views of the drawings.
The terms “including,” “comprising” and variations thereof, as used in this disclosure, mean “including, but not limited to,” unless expressly specified otherwise.
The terms “a,” “an,” and “the,” as used in this disclosure, mean “one or more,” unless expressly specified otherwise.
Devices that are in communication with each other need not be in continuous communication with each other, unless expressly specified otherwise. In addition, devices that are in direct contact with each other may contact each other directly or indirectly through one or more intermediary articles or devices. The device(s) disclosed herein may be made of a material such as, for example, a natural material, an artificial material, a polymer, a metal, a ceramic, an alloy, or the like (and/or various combinations thereof). For instance, the device(s) may be made of Polyether Ether Ketone (PEEK), silicon nitride (Si3N4) or its chemical analogs, titanium, a titanium alloy, or the like, or a combination of the foregoing. The material may be formed by a process such as, for example, an active reductive process of a metal (e.g., titanium or titanium alloy) and/or additive manufacturing (i.e., 3D printing) to create surface textures, which may include increasing the effective surface area and/or amount or extent of nanoscaled texture to device surface(s), so as to increase promotion of bone growth and fusion.
As previously noted, the various implant devices and/or components thereof disclosed herein can incorporate a silicon nitride material (i.e., Si3N4 and/or chemical analogues thereof) in their construction, either in the entirety of the implant as well as components, portions, layers and/or surfaces thereof. The incorporation of silicon nitride as a component material for spinal or other implants can provide significant improvements over existing implant materials and material designs currently available, as the silicon nitride material(s) will be highly osteo-inductive and/or osteoconductive and will desirably facilitate and/or promote implant fixation to adjacent living bone surfaces, while concurrently reducing and/or inhibiting periprosthetic infection and/or bacterial adhesion to the surfaces and/or interior portions of the implant
Silicon nitride (Si3N4) and its various analogs can impart both antibacterial and osteogenic properties to an implant, including to bulk Si3N4 as well as to implants coated with layers of Si3N4 of varying thicknesses. In bone replacement as well as prosthetic joint fusion and/or replacement, osseous fixation of implants through direct bone ingrowth (i.e., cementless fixation) is often preferred, and such is often attempted using various surface treatments and/or the incorporation of porous surface layers (i.e., porous Ti6Al4V alloy) on one or more bone-facing surfaces of an implant. Silicon nitride surfaces express reactive nitrogen species (RNS) that promote cell differentiation and osteogenesis, while resisting both gram-positive and gram-negative bacteria. This dual advantage of RNS in terms of promoting osteogenesis, while discouraging bacterial proliferation, can be of significant utility in a variety of implant designs.
Desirably, the inclusion of silicon nitride components into a given implant design will encompass the use of bulk silicon nitride implants, as well as implants incorporating other materials that may also include silicon nitride components and/or layers therein, with the silicon nitride becoming an active agent of bone fusion. RNS such as N2O, NO, and —OONO are highly effective biocidal agents, and the unique surface chemistries of Si3N4 facilitate its activity as an exogenous NO donor. Spontaneous RNS elution from Si3N4 discourages surface bacterial adhesion and activity, and unlike other direct eluting sources of exogenous NO, Si3N4 elutes mainly NH4+ and a small fraction of NH3 ions at physiological pH, because of surface hydrolysis and homolytic cleavage of the Si—N covalent bond. Ammonium NH4+ can enter the cytoplasmic space of cells in controlled concentrations and through specific transporters, and is a nutrient used by cells to synthesize building-block proteins for enzymes and genetic compounds, thus sustaining cell differentiation and proliferation. Together with the leaching of orthosilicic acid and related compounds, NH4+ promotes osteoblast synthesis of bone tissue and stimulates collagen type 1 synthesis in human osteoblasts. Conversely, highly volatile ammonia NH3 can freely penetrate the external membrane and directly target the stability of DNA/RNA structures in bacterial cells. However, the release of unpaired electrons from the mitochondria in eukaryotic cells activates a cascade of consecutive reactions, which starts with NH3 oxidation into hydroxylamine NH2OH (ammonia monooxygenase) along with an additional reductant contribution leading to further oxidation into NO2— nitrite through a process of hydroxylamine oxidoreductase. This latter process involves nitric oxide NO formation. In Si3N4, the elution kinetics of such nitrogen species is slow but continuous, thus providing long-term efficacy against bacterial colonies including mutants (which, unlike eukaryotic cells, lack mitochondria). However, when slowly delivered, NO radicals have been shown to act in an efficient signaling pathway leading to enhanced differentiation and osteogenic activity of human osteoblasts. Desirably, Si3N4 materials can confer resistance against adhesion of both Gram-positive and Gram-negative bacteria, while stimulating osteoblasts to deposit more bone tissue, and of higher quality.
Where the presence of bulk silicon nitride implant materials may not be desired and/or may be impractical for some reason, it may be desirous to incorporate modules and/or layers including silicon nitride on other materials, including in or on surface layers thereof. Silicon nitride structures and/or components can be formed using a variety of techniques, including by compressing, milling and firing silicon nitride powder, as well as by extruding silicon nitride into sheet, tube, pipe and/or thread form (which may be further processed into thread or “rope” by braiding and/or other techniques). Silicon nitride shapes may also be manufactured using subtractive manufacturing techniques (i.e., machining, milling and/or surface roughening), as well as by using additive manufacturing techniques (i.e., surface coating, brazing, welding, bonding, deposition on various material surfaces and/or even by 3D laser printing of structures). If desired, silicon nitride may even be formed using curing or other light/energy activation techniques, such as where a slurry of liquid polymer and silicon nitride particles may be UV cured to create a 3-dimensional structure and/or layer containing silicon nitride. In various embodiments, silicone nitride may be utilized in block form, in sheets, columns and bars, in cable or braided form, in mesh form, in a textured surface coating, in powder form, in granular form, in gel, in putty, in foams and/or as a surface filler and/or coating. In some cases, a surface layer of silicon nitride may be formed on an external and/or internal surface of an implant.
For example, in some embodiments it may be desirous to laser-sinter a thin layer of silicon nitride material (i.e., powder) to the surface of another material, such as PEEK or titanium. One exemplary starting micrometric powder used for laser-sintering of a Si3N4 coating in this manner could comprise a 90 wt % fraction of Si3N4 powder mixed with a 6 wt % of yttrium oxide (Y2O3) and a 4 wt % of aluminum oxide (Al2O3). If desired, a Vision LWI VERGO-Workstation equipped with a Nd:YAG laser with a wavelength of 1064 nm (max pulse energy: 70 J, peak power 17 kW, voltage range 160-500 V, pulse time 1-20 ms, spot size 250-2000 μm) can be utilized to achieve densification of successive layers of Si3N4 powder placed on a water-wet surface of a Titanium substrate in a nitrogen environment, which desirably limits Si3N4 decomposition and oxidation. In the exemplary embodiment, the Nd:YAG laser can be pulsed with a spot size of 2 mm, and driven by an applied voltage of 400 V with a pulse time of 4 ms. This operation can be repeated until a continuous thickness of 15 μm (±5 μm) is formed over an entire surface of the Titanium substrate. This process can create a wavy morphology of the ceramic/metal interface, with interlocks at the micrometer scale between metal and ceramic phases and desirably little or no diffusional transport of the Titanium element into the coating during laser sintering.
Any components of the cage structure may comprise a silicon nitride material, which may be combined in various embodiments with other materials such as, for example, a polymer, a metal, an alloy, or the like. For instance, the cage structure may comprise a central block structure made of PEEK, UHWMPE, titanium, chrome cobalt, stainless steel, a titanium alloy, or the like, with one or more outer surface layer(s) of silicon nitride to desirably increase promotion of bone growth and/or fusion in bone-contacting portions of the implant, as well as desirably reducing the potential for bacterial infection of the implant and/or the surgical site.
In other exemplary embodiments, silicon nitride materials of differing compositions and/or states (i.e., solid, liquid and/or flowable or moldable “slurry” states, for example) could be utilized in a single implant and/or portions thereof, including the use of solid silicon nitride for an arthroplasty cage implant, with a moldable silicon nitride “paste” placed within a centrally positioned “graft chamber” of the implant. In alternative embodiments, 3-D printing of silicon nitride materials (either solid or material mixes such as silicon nitride/PEEK precursors) can be utilized to create some or all of the various cage components described herein.
In various embodiments, the properties of the disclosed implants will desirably include improvements in one or more of the following: (1) Flexibility in manufacturing and structural diversity, (2) Strong, tough and reliable constructs, (3) Phase stable materials, (4) Favorable imaging characteristics, (5) Hydrophilic surfaces and/or structures, (6) Osteoconductive, (7) Osteoinductive, and/or (8) Anti-Bacterial characteristics.
Another significant advantage of using silicon nitride materials in bone implants is the anti-bacterial effects of the material on infectious agents. Upon implantation, a silicon nitride surface can induce an inflammatory response action which attacks bacterial biofilms near the implant. This reaction can also induce the elevation of bacterial pods above the implant surface by fibrin cables. Eventually the bacteria in the vicinity of the silicon nitride implant surfaces will be cleared by macrophage action, along with the formation of osteoblastic-like cells. In various experiments involving comparisons between standard implants and silicon nitride implants (both bulk and silicon nitride coated implants of standard materials), cell viability data in (which were determined at exposure times of 24 and 48 hours, showed the existence of a larger population of bacteria on the standard medical materials as compared to Si3N4 implants (both coated and bulk). A statistically validated decreasing trend for the bacterial population with time was detected on both coated and bulk substrates, with a highest decrease rate on Si3N4-coated substrates. Moreover, the fraction of dead bacteria at 48 h was negligible on the standard implants, while almost the totality of bacteria underwent lysis on the Si3N4 substrates. In addition, optical density data provided a direct assessment of the high efficacy of the Si3N4 surfaces in reducing bacterial adhesion.
In various embodiments, silicon nitride materials can be incorporated into a variety of implants and implant-like materials, including (1) orthopedic bone fusion implants (i.e., screws, cages, cables, rods, plugs, pins), (2) dental implants, (3) cranial/maxillofacial implants, (4) extremity implants, (5) hip and joint implants, (6) bone cements, powders, putties, gels, foams, meshes, cables, braided elements, and (7) bone anchoring elements and/or features. Where a surface coating of silicon nitride is added to an existing implant, such as to a titanium implant using a 3D-laser-sintering manufacturing process of deposition, this surface coating may comprise a dense, tenaciously adherent Si3N4 coating (with thickness 10-20 μm) onto the porous T-alloy surface of commercially available components, which may achieve rapid osseous fixation, while resisting bacteria.
Although process steps, method steps, or the like, may be described in a sequential order, such processes and methods may be configured in alternate orders. In other words, any sequence or order of steps that may be described does not necessarily indicate a requirement that the steps be performed in that order. The steps of the processes or methods described herein may be performed in any order practical. Further, some steps may be performed simultaneously.
When a single device or article is described herein, it will be readily apparent that more than one device or article may be used in place of a single device or article. Similarly, where more than one device or article is described herein, it will be readily apparent that a single device or article may be used in place of the more than one device or article. The functionality or the features of a device or article may be alternatively embodied by one or more other devices or articles which are not explicitly described as having such functionality or features.
Referring to
Referring to
In the cage structure 100, the first main surface 102 may include a surface pattern such as, for example, the surface pattern shown in
The surface pattern may be provided on any surface area, including that of a cage structure (e.g., cage structure 100), where bone cells can attach and grow, including, for example, external sagittal walls, external coronal walls (front and/or back), and the like. The surface pattern may be provided to any cage shape or form with, or without supplementary fixation features, including, for example, cages shapes/forms configured for ACIF, ALIF (see
The cage structure 100 may be configured to have a shape in a horizontal plane in the form of, for example, a rectangle, a trapezoid, a square, a pentagon, a circle, an oval, a hexagon, or any other shape that may be appropriate for a particular application, as understood by those skilled in the art. The cage structure 100 may be formed to substantially match the shape and/or size of the space between the adjacent vertebrae, as well as the shape and size of the vertebrae surfaces (e.g., vertebra 4 shown in
The cage structure 100 may include a plurality of side wall surfaces 104 that may extend between the first main surface 102 and the second main surface (not shown). The side wall surfaces 104 and the first and second main surfaces may form the outer shape of the cage structure 100. The plurality of side wall surfaces 104 may include, for example, a posterior wall surface 104A, an anterior wall surface 104B, and a pair of lateral (or side) wall surfaces 104C located opposite each other.
The cage structure 100 may include an opening 105. The opening 105 may be formed in or near the center portion of the cage structure 105. The opening 105 may extend between the superior and inferior directions of the cage structure 100, extending from the first main surface 102 to the second main surface (not shown). The opening 105 may be defined and laterally surrounded by inner wall surface(s) 106 of the cage structure 100. The opening 105 may form a chamber, such as, for example, a graft chamber that is configured to receive, for example, blood, tissue, bone, bone graft and the like, to promote bone growth or fusion. The inner wall surfaces 106 may have a surface pattern (not shown) that may help in retaining blood, tissue, bone graft, etc., in the graft chamber.
The cage structure 100 may include one or more openings or windows (not shown), such as, for example, window(s) 299 shown in
As seen in
Referring to
Following a discectomy procedure, a medical professional may determine an appropriate size of the cage structure 100 by selecting an appropriately dimensioned cage structure 100 and an appropriately dimensioned plating device (not shown), if applicable, which may be selectable based on, for example, height, width, depth, and the like. Upon selecting the appropriate cage structure 100 (and plating device, if applicable), one or more of an ACIF, ALIF, PLIF, TLIF, DLIF, OLIF, VBR, or the like may be performed by placing the cage structure 100 between adjacent vertebrae 4 in the space formed by the removed degenerated disc. Placement of the cage structure 100 within the spinal column may prevent spaces between adjacent vertebrae 4 from collapsing, thereby preventing adjacent vertebrae from resting immediately on top of one another and inducing fracture of vertebra 4, impingement of the spinal cord, and/or pain. Additionally, such cage structures 100 may facilitate fusion (e.g., bone to grow together) between adjacent vertebrae 4 by stabilizing adjacent vertebrae 4 relative to one another and promoting bone ingrowth.
Referring to
The hole 108A may be located, for example, at the center of the wall surface 104B. The hole 108A may have a larger diameter than the hole 108B. The hole 108A may be threaded to engage the threaded end 432 of the implant tool 400. The hole 108B may be constructed to engage the orientation guide 434 of the implant tool 400. The hole 108A may be deeper than the hole 108B.
Once the implant tool 400 is securely and fixedly attached to the cage structure 100, the surgeon may align and implant the cage structure 100 in the space prepared for implanting of the cage structure 100. If applicable, the surgeon may implant a plating device 50C (see
In some optional embodiments, the cage structure 100 may include a wall portion 106A that may be bulged inwardly to provide added strength for the area surrounding the hole 108A, so as to be able receive and withstand substantial force that may be applied to the cage structure 100 through the implant tool 400.
Referring to
The main body 110 and/or the first and second plates 150A, 150B may be formed of one or more robust, strong and ductile materials, such as, for example, a polymer, a metal, an alloy, or the like. For example, the main body 110 may be formed of PEEK or a ceramic such as silicon nitride, and the first and second plates 150A, 150B may be formed of titanium or a titanium alloy. The main body 110 and the first and second plates 150A, 150B may be a single unitary piece or an assembly of two or more parts that are independently produced.
As seen in
The first and second plates 150A, 150B may be attached to the first surface 112 and the second surface (not shown) of the main body 110, respectively. The main body 110 may be vertically and/or horizontally symmetric, in which case the first surface 112 may be configured to contact either or both of the surfaces of the first and second plates 150A, 150B. The first and second plates 150A, 150B may have substantially the same shape and construction, and hence may be interchangeably used. Alternatively, the first surface 112 and the second surface (not shown) of the main body 110 may have different shapes and constructions; and, the first and second plates 150A, 150B may be shaped and constructed differently to fit to the first surface 112 and the second surface, respectively.
The main body 110 may have an opening 105A (shown in
As seen in
The first and second plates 150A, 150B may be attached to the main body 110 by an adhesive, a fastener, or the like. For example, the first plate 150A may be adhered to or snapped in the main body 110. Alternatively or additionally, the first and second plates 150A, 150B may be attached to the main body 110 by one or more fasteners, such as, for example, a pin, a screw, a rivet, a bolt, a nut, or the like. For example, the main body 110 may include one or more pin holes 117 (three shown in
Alternative or additionally, the main body 110 and the first and second plates 150A, 150B may be constructed to structurally engage each other. For example, the first surface 112 of the main body 110 may have a wall 120 protruding upwardly and extending along a periphery of the first surface 112. As seen in
Additionally, the main body 110 may have one or more recesses 122, and the first and second plates 150A, 50B may have one or more tabs 158, which may be located and shaped to fit into the recesses 122 of the main body 110. For example, as seen in
The first plate 150A may have one or more cutouts 156 (two shown) and one or more push tabs 160 (more clearly shown with the second plate 150B in
The outer surface 152 of the first and second plates 150A, 150B may have a surface pattern 170 that may form the first main surface 102 and/or the second main surface (not shown). The surface pattern 170 may establish and promote bone growth and resist movement (e.g., departure, slippage, etc.) installed with respect to a vertebra. The surface pattern 170 may include a symmetrical geometric pattern (e.g., circle, sphere, semi-sphere, equilateral triangle, pyramid, isosceles triangle, square, rectangle, kite, rhombus, pentagon, hexagon, heptagon, octagon, or the like), an asymmetrical geometric pattern (e.g., irregular sphere or semi-sphere, scalene triangle, irregular pyramid, irregular quadrilateral, irregular pentagon, irregular hexagon, irregular heptagon, irregular octagon, or the like), a combination of one or more symmetrical geometric patterns and/or one or more asymmetrical geometric patterns, and/or the like. The surface pattern 170 may be formed by, for example, machining, chemically machining, and/or stamping the outer surface 152. Alternatively or additionally, the outer surface 152 may be chemically processed by performing micro-surface treatments, such as, for example, chemical etching, hydroxyapatite coating, and/or the like. AS another alternative, the surface may be created using 3-D additive “printing” technologies, as known in the art. The surface pattern 170 may have a structure shown in
The cage structure may include one or more openings or windows such as, for example, window(s) 299C. The window(s) may be formed in the lateral, posterior and/or anterior walls. Such windows may remain empty and/or may be filled with radiolucent material such as tissue grafts as will be described in further detail below. The windows may enable a medical professional to view and/or determine the level of post-operative fusion between cage structure and patient bone and/or tissue. The cage structure body may define any appropriate arrangement, number, and configuration of windows. As seen in the example in
The cage structure 100C may include one or more holes 108C and/or recessed portions 109C. If desired, the holes may or may not include internally threaded sections, which in some embodiments may allow for connection of the cage structure 100C to supplemental plates (see
It should be understood that the various patterns shown in
Referring to
As best seen in
As seen in
As shown in
Referring to
The cage structure 200 may include an opening 240, which may extend from the first surface 202 to the second surface 204. The opening 240 may be a graft chamber, or the like, similar to the opening 105 (shown in
The first and second surfaces 202, 204 may have a surface pattern 270, which may be configured to directly contact a surface of the adjacent vertebra during implantation. The surface pattern 270 may establish and promote bone growth and resist movement (e.g., departure, slippage, or the like). In various embodiments, a desired surface texture may include one or more of the following: (1) creation of a high friction surface area with increased resistance to expulsion due to increased surface area and/or harp edges gripping, (2) induces “rasping” of boney surfaces by sharp edges during implant insertion and/or movement to induce a bleeding pathway without significantly weakening the vertebral endplate (i.e., leaving it substantially intact—which is highly desirable for fusion), (3) having the width of the peak greater than the width of the root of the peak, thereby forming a “v” pattern, and/or (4) providing a dramatically increased surface area as compared to a non-textured surface—in some case more than 130% of the surface area for bone adhesions and growth as compared to typical pyramidal shaped patterns—which allows for cage to held in plate when pressed against low density foam against normal gravitational attraction.
The protrusions 272 may include a pocket 278, which may be a hole or a slot formed at a superior (or inferior) surface 279 thereof, to increase a bone growth area. The superior surfaces 279 may have one or more symmetric geometry shapes, one or more asymmetric geometry shapes, a combination of a symmetric geometry shape and an asymmetric geometry shape, or the like. Two neighboring protrusions 272 may have different superior surface shapes.
As best seen in
Desirably, the two-cut orientation for each groove 2000 creates two grooves separated by an upside-down V cut (i.e., a peak or “bottom level pyramid”—see
If desired, the alternative tooth pattern of
In various alternative embodiments, the pattern of
In various alternative embodiments, one or more of the following may apply: (1) the gap at the peak may be equal or greater than 3 mm, (2) the peak gap and valley gap ration [B/D] may be between 0.3 and 1.0, (3) the peak depression depth [C] may be between 0 and 1 mm, (4) the depth of the valley may be may be grater than the peak depression depth [C] and less than 2 mm, (5) the angle of the upside-down V may be between 0 and 120 degrees, (6) the angle of the peak depression (looks like a female “V”) may be between 0 and 91 degrees, (7) the cutter disc edge may be flat or pointed, with the base of the valley per such tool being flat or pointed, and/or (8) the obtuse and acute angles formed post cut may have sharp radii between 0 and 0.3 mm.
In some embodiments, only a single orientation for parallel cutting passes may be sufficient to create a desired surface geometry. For example, in the embodiments of
As seen in
For example, as seen in
The surface layers 214A, 214B may be attached to outer surfaces of the wing portions 212B, 212C, respectively, or the surface layers 214A, 214B may be integrally formed with the wing portions 212B, 212C. The surface layers 214A, 214B may include the first and second surfaces 202, 204, respectively. Inner surfaces of the bridge portion 212A and the wing portions 212B, 212C may be smooth and clean to reduce friction when the insertion 250 is inserted to a space surrounded by the shell 210.
The shell main body 212 may be formed of one or more materials that may provide a visible fusion window. For example, the shell main body 212 may be formed of a plastic material such as PEEK or the like. Alternatively, the shell main body may be formed of a bone growth promoting ceramic material such as silicon nitride or the like (or combinations of such materials, including silicon nitride/PEEK combinations). The surface layers 214A, 214B may be formed of one or more materials that can be processed to form the surface pattern 270 having, for example, undercut 276, pocket 278, and/or the like. For example, the surface layers 214A, 214B may be formed of titanium, a titanium alloy, or the like.
The shell 210 of the cage structure 200 may be used alone as a cage, without any other parts. For example, as seen in
The insertion body 250 may be constructed to fit into a space surrounded by the shell 210. As seen in
The insertion body 250 may be formed of metal (e.g., titanium, a titanium alloy, or the like), a radiopaque or radiolucent material (e.g., PEEK), an elastic and/or shock-absorbing material (e.g., silicon), a ceramic material such as silicon nitride (Si3N4), an allograft bone, or the like. The insertion 250 may be a single unitary piece or a combination of multiple pieces that are manufactured separately. As noted earlier, the insertion body 250 may include one or more windows, such as, for example, window 299 shown in
The shell 210 and the insertion body 250 may be assembled together by an adhesive, a fastener, or the like. For example, the shell 210 and the insertion body 250 may be glued together. Alternatively or additionally, the shell 210 may be attached to the insertion body 250 by one or more fasteners, such as, for example, a pin, a screw, a rivet, a bolt, a nut, or the like.
For example, as seen in
The shell 210 and the insertion body 250 may be constructed to mate to each other and form a unitary structure. For example, one or more slots 256 (e.g., two shown in
The cage structure(s) described herein, including cage structure 200 (or 100) may include additional features, constructed according to the principles of the disclosure. For instance, the cage structures described herein may include one or more anchoring ears that may be integrally formed with the cage structures.
Referring to
The cage structure 200 may be modified to include screw holes without adding the bone anchoring ears 260A, 260B shown in
Referring to
The cage shell 210′ may be implanted in a patient using a process similar to that described for the interbody device 410 or interbody system 400 described in U.S. patent application Ser. No. 15/244,868, filed Aug. 23, 2016 and entitled “Modular Plate and Cage Elements and Related Methods,” the entirety of which is incorporated herein by reference, with references to FIGS. 18A-18C of that application.
As seen in
The holes 218A, 218B may extend inwardly from the anterior surface 206B to engage, for example, the implant tool 400 (shown in
The cage structure may include one or more openings 240, which may extend from the first surface 202 to the second surface 204. The opening 240 may be a graft chamber, as discussed above. As seen in
The first and second surfaces 202, 204 may have a surface pattern 270, which may be configured to directly contact a surface of the adjacent vertebra during implantation. The surface pattern 270 may establish and promote bone growth and resist movement (e.g., departure, slippage, or the like), as described above.
The mounting plate 320 may include a plurality of screw holes which extend from the first main surface 322 to the second main surface (not shown). For example, one or more screw holes 324A (two shown) may be formed at the upper portion 320A, and one or more screw holes 324B (two shown) may be formed at the lower portion 320B. The screw holes 324A formed at the upper portion 320A may be slanted upwardly to direct bone screws (not shown) inserted thereto further up from a bottom of the vertebrae 4A. The screw holes 324B formed at the lower portion 320B may be slanted downwardly to direct bone screws (not shown) inserted thereto further down from a top of the vertebrae 4B. The insertion portion 310 and the mounting plate 320 may be integrally formed, or, alternatively, produced independently from each other and assembled together.
Referring to
As shown in
The holes 1218A, 1218B may extend inwardly from the anterior surface 1206B to engage, for example, an implant tool (as previously described) or the like. The cage structure 1200 may include an opening 1240, which may extend from the first surface 1202 to the second surface 1204. The opening 1240 may be a graft chamber, and may be formed at, for example, a center portion of the cage structure 1200. The opening 1240 may be laterally surrounded and defined by an inner wall surface 1216.
The cage structure 1200 may include one or more surface layers 1214A, 1214B or textures, as described herein. One or more portions of a shell 1212 of the cage 1200 may have one or more guides 1236 formed corresponding to one or more slots (not shown) in an insertion body. As previously described, the guides 1236 may be tapered to fit tapered slots of an insertion body.
For example,
As previously noted,
While the disclosure has been described in terms of exemplary embodiments, those skilled in the art will recognize that the disclosure can be practiced with modifications in the spirit and scope of the appended claim, drawings and attachment. The examples provided herein are merely illustrative and are not meant to be an exhaustive list of all possible designs, embodiments, applications or modifications of the disclosure.
Note that, in various alternative embodiments, variations in the position and/or relationships between the various figures and/or modular components are contemplated, such that different relative positions of the various modules and/or component parts, depending upon specific module design and/or interchangeability, may be possible. In other words, different relative adjustment positions of the various components may be accomplished via adjustment in separation and/or surface angulation of one of more of the components to achieve a variety of resulting implant configurations, shapes and/or sizes, thereby accommodating virtually any expected anatomical variation. For example, variation of the thicknesses and/or separation distance between various surfaces (i.e., optionally without altering the angulation of the surfaces) can desirably cause an increase or decrease in the size or “height” of the implant, due to changes in the z-axis positioning of the components which engage the adjacent vertebrae. Concurrently, alterations in the “tilt angle” or angulation of one or both of the surfaces or other components in the medial-lateral (i.e., rotation about a y-axis) and/or anterior-posterior (i.e., rotation about an x-axis) axes of the implant will allow the implant to be utilized to accommodate a wide variety of natural and/or surgically altered surfaces of the spine. Moreover, various complex combinations (at various amounts) of comparative lateral (e.g., left-right) tilt and fore-aft (e.g., anterior-posterior) tilt can be accomplished, with or without concurrent adjustments in the various cutting surfaces.
The various embodiments of an implant disclosed herein can be configured to interact with two bone vertebrae of a spine or other anatomical locations. The spine may have any of several types of spinal curvature disorders which are sought to be treated. Examples of such spinal curvature disorders include, but need not be limited to, lordosis, kyphosis, scoliosis and/or low and/or high velocity fractures, among other pathologies.
In various exemplary scenarios, a variety of surgical tools can be used in conjunction with various implant devices utilized to fix and/or secure adjacent vertebrae that have had cartilaginous disc between the vertebrae replaced with fusion material that promotes the fusion of the vertebrae, such as a graft of bone tissue. Also, such can be accomplished even when dealing with a spinal curvature disorder (e.g., lordosis, kyphosis and scoliosis).
Of course, method(s) for manufacturing the surgical devices and related components and implanting an implant device into a spine are contemplated and are part of the scope of the present application.
While embodiments and applications of the present subject matter have been shown and described, it would be apparent to those skilled in the art that many more modifications are possible without departing from the inventive concepts herein. The subject matter, therefore, is not to be restricted except in the spirit of the appended claims.
All references, including publications, patent applications, and patents, cited herein are hereby incorporated by reference to the same extent as if each reference were individually and specifically indicated to be incorporated by reference and were set forth in its entirety herein.
The various headings and titles used herein are for the convenience of the reader and should not be construed to limit or constrain any of the features or disclosures thereunder to a specific embodiment or embodiments. It should be understood that various exemplary embodiments could incorporate numerous combinations of the various advantages and/or features described, all manner of combinations of which are contemplated and expressly incorporated hereunder.
The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The terms “comprising,” “having,” “including,” and “containing” are to be construed as open-ended terms (i.e., meaning “including, but not limited to,”) unless otherwise noted. Recitation of ranges of values herein are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., i.e., “such as”) provided herein, is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.
Preferred embodiments of this invention are described herein, including the best mode known to the inventor for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventor expects skilled artisans to employ such variations as appropriate, and the inventor intends for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or otherwise clearly contradicted by context.
This application is a continuation-in-part of U.S. patent application Ser. No. 16/505,096 entitled “ACIF CAGE, CAGE SYSTEM AND METHOD,” filed Jul. 8, 2019, which is a continuation-in-part of U.S. patent application Ser. No. 15/220,090 entitled “ACIF CAGE, CAGE SYSTEM AND METHOD,” filed Jul. 26, 2016, the disclosures of which are each incorporated by reference herein in their entireties. This application further claims the priority of U.S. Provisional Patent Application 63/063,853 entitled “CAGE SYSTEM AND METHODS FOR ENHANCED BONE INTERFACE AND GROWTH,” filed Aug. 10, 2020, the disclosure of which is incorporated by reference herein in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 63063853 | Aug 2020 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16505096 | Jul 2019 | US |
| Child | 17398984 | US | |
| Parent | 15220090 | Jul 2016 | US |
| Child | 16505096 | US |
