# US 11,896,498 B2 · Interbody fusion devices and related methods of manufacture

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- Number: US 11,896,498 B2
- Document ID: US11896498B2
- Status: Granted
- Kind: B2
- Application number: 17/571,810
- Filed: 2022-01-10
- Published: 2022-07-28
- Granted: 2024-02-13
- Earliest claimed: 2016-09-16
- Assignees: MiRus LLC
- Applicants: Mirus LLC
- Inventors: Wayne Gray; Antonio Terrell; Clint Walker; Kevin R. Strauss; Ryan O'Flaherty; Noah Roth
- Web page: https://patentgrep.com/patent/US11896498B2

## CPC

- A61F 2/4465: {having a circular or kidney shaped cross-section substantially perpendicular to the axis of the spine}
- A61F 2/4455: {for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages (intervertebral discs A61F2/442)}
- A61F 2/447: {substantially parallelepipedal, e.g. having a rectangular or trapezoidal cross-section}
- A61F 2002/30028: {differing in tissue ingrowth capacity, e.g. made from both ingrowth-promoting and ingrowth-preventing parts}
- A61F 2002/3006: {Properties of materials and coating materials}
- A61F 2002/30154: {square}
- A61F 2002/30593: {hollow}
- A61F 2002/30677: {Means for introducing or releasing pharmaceutical products, e.g. antibiotics, into the body}
- A61F 2002/30784: {Plurality of holes}
- A61F 2002/30838: {Microstructures}
- A61F 2002/30878: {with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts}
- A61F 2002/30904: {serrated profile, i.e. saw-toothed}
- A61F 2002/3093: {for promoting ingrowth of bone tissue}
- A61F 2310/00389: The prosthesis being coated or covered with a particular material
- A61F 2310/00592: Coating or prosthesis-covering structure made of ceramics or of ceramic-like compounds
- A61F 2310/00796: Coating or prosthesis-covering structure made of a phosphorus-containing compound, e.g. hydroxy(l)apatite
- A61F: FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS (dental prosthetics A61C)

## Abstract

Interbody fusion devices and related methods of manufacture are described herein. An example interbody fusion device can include a plurality of vertebral endplates, and a body extending between the vertebral endplates. The body and the vertebral endplates can define an internal cavity. Additionally, each of the vertebral endplates can include a lattice structure and a frame surrounding the lattice structure, where the lattice structure being configured to distribute load. Each of the vertebral endplates can also include a plurality of micro-apertures having an average size between about 2 to about IO micrometers (μm), and a plurality of macro-apertures having an average size between about 300 to about 800 micrometers (μm).

## Claims

### Claim 1

An interbody fusion device comprising top and bottom endplates, first and second lateral sides, anterior and posterior ends, and a body; said body positioned between said top and bottom endplates, said first and second lateral sides, and said anterior and posterior ends; each of said top and bottom endplates configured to interface or engage with bone when said interbody fusion device is positioned between adjacent vertebra of a spine; said body includes a body cavity; said first lateral side includes a plurality of first lateral openings that terminate in said body cavity; said second lateral side includes a plurality of second lateral openings that terminate in said body cavity; cavity; said posterior end includes a first posterior opening that terminates in said body cavity; said anterior end absent an opening that terminates in said body cavity; said top endplate is formed of a top lattice structure and a top frame surrounding said top lattice structure; said bottom endplate is formed of a bottom lattice structure and a bottom frame surrounding said bottom lattice structure; said top lattice structure on said top endplate forming a plurality of top openings that terminate in said body cavity; said bottom lattice structure on said bottom endplate forming a plurality of bottom openings that terminate in said body cavity; said top frame of said top endplate includes a top micro-aperture region that fully encircles said top lattice structure; said top micro-aperture region includes a plurality of top micro-apertures having an average size of 2-10 micrometers (μm) and a plurality of top macro-apertures having an average size of 300-800 micrometers (μm); one or more of said top micro-apertures terminating in said body cavity; one or more of said top macro-apertures terminating in said body cavity; each of said top openings has a size that is greater than each of said top micro-apertures and each of said top macro-apertures; said bottom frame of said bottom endplate includes a bottom micro-aperture region that fully encircles said bottom lattice structure; said bottom micro-aperture region includes a plurality of bottom micro-apertures having an average size of 2-10 micrometers (μm) and a plurality of bottom macro-apertures having an average size of 300-800 micrometers (μm); one or more of said bottom micro-apertures terminating in said body cavity; one or more of said bottom macro-apertures terminating in said body cavity; each of said bottom openings has a size that is greater than each of said bottom micro-apertures and each of said bottom macro-apertures.

### Claim 2 (depends on 1)

The interbody fusion device as defined in claim 1, wherein a majority of said top openings has a same shape; and a majority of said bottom openings has a same shape.

### Claim 3 (depends on 2)

The interbody fusion device as defined in claim 2, wherein a majority of said top openings has a square shape along a longitudinal length of said top opening; and a majority of said bottom openings has a square shape along a longitudinal length of said bottom opening.

### Claim 4 (depends on 3)

The interbody fusion device as defined in claim 3, wherein a majority of said top openings include angled corners; and a majority of said bottom openings include angled corners.

### Claim 5 (depends on 4)

The interbody fusion device as defined in claim 4, wherein each of said top and bottom endplates includes a plurality of teeth.

### Claim 6 (depends on 5)

The interbody fusion device as defined in claim 5, wherein each of said first and second lateral sides has a curved profile along a complete longitudinal length of said first and second lateral sides; said anterior end has a curved profile along a complete width of said anterior end.

### Claim 7 (depends on 6)

The interbody fusion device as defined in claim 6, wherein first posterior opening extends a full width of said posterior end.

### Claim 8 (depends on 7)

The interbody fusion device as defined in claim 7, wherein said top and bottom endplates, said first and second lateral sides, and said anterior and posterior ends formed of one or more materials selected from the group consisting of a) demineralized bone matrix (DBM), b) autograft bone, c) allograft bone, d) stem cells, e) synthetic material; f) titanium; g) titanium alloy; g) cobalt chrome alloy; i) stainless steel; j) molybdenum rhenium (MoRe) alloy; k) polyether ether ketone (PEEK); l) polyaryletherketone (PAEK); m) poly(methyl methacrylate) (PMMA); and n) carbon fiber.

### Claim 9 (depends on 8)

The interbody fusion device as defined in claim 8, wherein one or both of said top endplate and said bottom endplate includes a fusion promoting or infection prevention coating layer; said fusion promoting or infection prevention coating layer includes one or more materials selected form the group consisting of a) hydroxyapatite, b) bone morphogenetic protein (BMP), c) antibiotic, d) porous coating, e) hydrophilic coating, and f) silver zeolite.

### Claim 10 (depends on 2)

The interbody fusion device as defined in claim 2, wherein a majority of said top openings include angled corners; and a majority of said bottom openings include angled corners.

### Claim 11 (depends on 1)

The interbody fusion device as defined in claim 1, wherein each of said top and bottom endplates includes a plurality of teeth.

### Claim 12 (depends on 1)

The interbody fusion device as defined in claim 1, wherein each of said first and second lateral sides has a curved profile along a complete longitudinal length of said first and second lateral sides; said anterior end has a curved profile along a complete width of said anterior end.

### Claim 13 (depends on 1)

The interbody fusion device as defined in claim 1, wherein first posterior opening extends a full width of said posterior end.

### Claim 14 (depends on 1)

The interbody fusion device as defined in claim 1, wherein said top and bottom endplates, said first and second lateral sides, and said anterior and posterior ends formed of one or more materials selected from the group consisting of a) demineralized bone matrix (DBM), b) autograft bone, c) allograft bone, d) stem cells, e) synthetic material; f) titanium; g) titanium alloy; g) cobalt chrome alloy; i) stainless steel; j) molybdenum rhenium (MoRe) alloy; k) polyether ether ketone (PEEK); l) polyaryletherketone (PAEK); m) poly(methyl methacrylate) (PMMA); and n) carbon fiber.

### Claim 15 (depends on 1)

The interbody fusion device as defined in claim 1, wherein one or both of said top endplate and said bottom endplate includes a fusion promoting or infection prevention coating layer; said fusion promoting or infection prevention coating layer includes one or more materials selected form the group consisting of a) hydroxyapatite, b) bone morphogenetic protein (BMP), c) antibiotic, d) porous coating, e) hydrophilic coating, and f) silver zeolite.
