Laser-produced porous surface

Information

  • Patent Grant
  • 11918474
  • Patent Number
    11,918,474
  • Date Filed
    Friday, June 12, 2020
    3 years ago
  • Date Issued
    Tuesday, March 5, 2024
    a month ago
Abstract
A method of forming an implant having a porous tissue ingrowth structure and a bearing support structure. The method includes depositing a first layer of a metal powder onto a substrate, scanning a laser beam over the powder so as to sinter the metal powder at predetermined locations, depositing at least one layer of the metal powder onto the first layer and repeating the scanning of the laser beam.
Description
BACKGROUND OF THE INVENTION

The present invention relates to a device having a porous surface attached directly or indirectly to a bearing surface and a method for forming the same.


In particular, this invention relates to a computer-aided laser apparatus or other suited high energy beam, which sequentially remelts a plurality of powder layers to build a porous layer in a layer-by-layer fashion.


The present invention also includes a method of attaching or connecting a bearing surface directly or indirectly preferably formed from a polymer to the sequentially-built porous part.


The present application is particularly directed toward a method of forming a porous and partially-porous metallic structure having a bearing surface.


The field of free-form fabrication has seen many important recent advances in the fabrication of articles directly from computer-controlled databases. These advances, many of which are in the field of rapid prototyping of articles such as prototype parts and mold dies, have greatly reduced the time and expense required to fabricate articles, particularly in contrast to conventional machining processes in which a block of material, such as a metal, is machined according to the engineering drawings. One example of a modern rapid prototyping technology is the selective laser sintering process practiced by systems available from 3D Systems, Valencia, California According to this technology, articles are produced in a layer-wise fashion, from a laser-fusible powder that is dispensed one layer at a time. The powder is fused, remelted or sintered, by the application of laser energy that is directed in raster-scan fashion to portions of the powder layer corresponding to a cross-section of the article. After fusing of the powder on one particular layer, an additional layer of powder is dispensed, and the process repeated with fusion taking place between the current layer and the previously laid layers, until the article is complete.


The field of rapid prototyping of parts has, in recent years, made large improvements in broadening high strain, high density parts for use in the design and pilot production of many useful articles including metal parts. These advances have permitted the selective laser remelting and sintering process to now also be used in fabricating prototype tooling for injection molding, with expected tool life in excess of 10,000 mold cycles. The technologies have also been applied to the direct fabrication of articles, such as molds from metal powders without a binder. Examples of metal powder reportedly used in such direct fabrication include two-phase metal powders of the copper-tins, copper-solder (the solder being 70% lead and 30% tin), and bronze-nickel systems. The metal articles formed in these ways have been quite dense, for example, having densities of up to 70% to 80% of full density (prior to any infiltration). Prior applications of this technology have strived to increase the density of the metal structure formed by the melting or sintering process. The field of rapid prototyping of parts has focused on providing high strength, high density parts for use and design in production of many useful articles, including metal parts.


But while the field of rapid prototyping has focused on increasing density of such three-dimensional structures, the field has not focused its attention on reducing the density of three-dimensional structures. Consequently, applications where porous and partially-porous metallic structures, and more particularly metal porous structures with interconnective porosity, are advantageous for use, have been largely ignored.


In addition, many structures, especially in the medical arts, require two different surfaces, each adapted for their own purposes. Along this line, a structure may have a first surface which needs to be porous for tissue in-growth and a second surface which should be adapted to be a bearing surface. Further, the first surface or portion may include different layers having different gradients of porosity. For example, the first surface may include an outer region having a porosity of approximately 80%. As you move normal with regard to the first surface the porosity may alter such that the porosity is increased or in a preferred embodiment, the porosity decreases even until the porosity is almost zero. Of course, the present invention contemplates a situation where the porosity alters from position to position depending on the requirements of the device.


Although different techniques have tried to provide such a method and apparatus, still greater techniques are needed in this area.


SUMMARY OF THE INVENTION

In one embodiment, the present invention relates to a method of forming an implant having a porous tissue ingrowth structure and a bearing support structure. The method may include depositing a first layer of a metal powder onto a substrate. Next, a laser beam scans over the powder so as to sinter the metal powder at predetermined locations. At least one layer of the metal powder may be deposited onto said first layer while repeating the laser scanning step for each successive layer until a predetermined structure having a first surface and a second surface is constructed. A flowable polymer is placed into contact with the second surface of said predetermined structure. The polymer is cooled such that the flowable polymer adheres to the second surface of the structure. The laser scanning step may include scanning the laser beam onto the metal powder to form a portion of a plurality of predetermined unit cells within the metal powder.


The method may include placing the predetermined structure into a cavity of a die and depositing a polymer onto the second surface of the predetermined structure within the cavity of the die. The step of placing a flowable polymer in contact with the second surface of the predetermined structure may include applying pressure and heat to the polymer in the cavity of the die. The step of placing the flowable polymer in contact with the second surface of the predetermined structure may include transferring the flowable polymer onto the second surface. The step of placing the flowable polymer in contact with the second surface of the predetermined structure may include placing the second surface of the predetermined structure adjacent a polymer structure, applying heat to the polymer structure and allowing the polymer structure to engage the predetermined structure. The predetermined structure may include an outer layer, an intermediate layer and an inner layer, the outer layer and the inner layer being relatively porous and the intermediate layer being relatively dense such that the flowable polymer cannot substantially leech through the intermediate layer from the inner layer to the outer layer. The outer layer has a porosity approximately between 60% to 80% and the inner layer has a porosity approximately higher than 80%. The outer layer may have a pore size distribution in the range of 80 μm to 800 μm and the inner layer may have a pore size distribution higher than approximately 800 μm.


The predetermined structure may have a gradient porosity. The gradient porosity of the predetermined structure may include a first layer that is substantially porous, a second layer that is substantially non-porous, a third layer that is substantially porous such that the flowable polymer cannot substantially leech through the second layer from the third layer to the first layer when the flowable liquid polymer is placed in contact with the third layer.


The present invention also includes a medical implant including a metal insert having a bone ingrowth structure, an intermediate structure and a bearing support structure, the bone ingrowth structure having a porosity sufficient to promote bone ingrowth. The implant also includes a bearing surface formed from a polymer material, the bearing surface being attached to the bearing support structure. The intermediate structure has a porosity sufficient to inhibit the polymer material from translating through the bearing support structure to the bone ingrowth structure. The intermediate structure may be designed to facilitate a specific stiffness characteristic to an overall construct and/or include two barrier layers and a bridging section.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1A is one embodiment of a metal insert of an acetabular cup constructed according to the present invention;



FIG. 1B illustrates a cut out portion of the metal insert of FIG. 1A;



FIG. 1C is a unit cell used to construct a portion of the metal insert of FIG. 1A;



FIG. 1D is a computer model of a portion of an acetabular cup constructed using the unit cell of FIG. 1C;



FIG. 1E is a unit cell used to construct a portion of the metal insert of FIG. 1A;



FIG. 1F is a computer model of a portion of an acetabular cup constructed using the unit cell of FIG. 1E;



FIG. 1G is a computer rendering of an acetabular cup including the portions illustrated in FIGS. 1D and 1F;



FIG. 2 is a schematic drawing of a pelvis region;



FIG. 3 is a schematic drawing of an acetabular cup and a femoral stem implanted into the pelvic region;



FIG. 4 is an illustration of an apparatus used in conjunction with the present invention;



FIG. 5 illustrates an alternate apparatus for employing methods of the present invention;



FIG. 6 is a sample of constructed coupons using a method according to the present invention;



FIG. 7 is a table showing a series of parameters used for making samples according to the present invention;



FIGS. 8A-8C are scanning electro-microscopic images of the surface structure of various samples made by a method according to the present invention;



FIG. 9A-9D are illustrations of different embodiments of unit cells according to the present invention;



FIG. 10 illustrates a lattice structure using a plurality of unit cells according to FIG. 8A;



FIG. 11 illustrates a lattice structure with and without laser beam compensation using the unit cells illustrated in FIG. 1;



FIG. 12 illustrates a lattice structure using a plurality of unit cells illustrated in FIG. 8B;



FIG. 13 illustrates a lattice structure with and without laser beam compensation using the unit cell of FIG. 8B;



FIG. 14 illustrates a lattice structure using a plurality of unit cells illustrated in FIG. 8C;



FIGS. 15A and 15B illustrate lattice structures created using unit cells illustrated in FIGS. 9D and 8A with varying exposure time, respectively;



FIG. 15C illustrates a side view of the embodiment of FIG. 15A;



FIG. 15D illustrates a side view of the lattice structure illustrated in FIG. 15B;



FIG. 16 is a representation of a lattice structure created using a plurality of unit cells illustrated in FIG. 8D with random perturbation;



FIG. 17 is an illustration of an acetabular cup built using the methods of the present invention;



FIG. 18 is an illustration of an alternate embodiment of an acetabular cup built using the methods of the present invention;



FIG. 19 is an illustration of an alternate embodiment of an acetabular cup built using the methods of the present invention;



FIGS. 20 and 21 are representations of a patella component built using one embodiment of the present invention.



FIG. 22 is a side view of a cartilage plug built according to one embodiment of the present invention;



FIG. 23 is a front view of the cartilage plug of FIG. 22; and



FIG. 24 is an illustration of an alternate embodiment of an acetabular cup.





DETAILED DESCRIPTION

The present invention relates to a method of forming a porous or partially porous metallic structure having a bearing surface attached directly or indirectly thereto. The structures are particularly but not exclusively applicable for use in the art of soft tissue interlock structures for medical implants and prosthesis.


The method makes use of laser technology or any other high energy beam by employing a variety of scanning strategies.


Typical metal and metal alloys employed include stainless steel, cobalt chromium alloys, titanium and its alloys, tantalum and niobium, all of which have been used in medical device applications. The present invention can be used for such medical device applications where bone and/or soft tissue interlock with the component is required, or where a controlled structure is required to more closely match mechanical properties of the device with surrounding tissue.


Additionally, the present invention may be employed to enhance the biocompatibility of a porous structure with human tissue while also providing a bearing surface that is resistant to wear. With these advantages in mind, a structure may be created using specific dimensions required to accommodate a particular patient.


The porous and partially porous metallic structures may be attached or incorporated to a surface, which will be used as a bearing surface, as is described below. By interconnecting or having an implant with a porous structure adjacent a bearing surface, the orthopedic implant can provide a structure for permitting bone and soft tissue interlock in combination with a bearing surface that enables the implant to rotate, articulate or pivot relative to an additional bearing surface.


As shown in FIGS. 1A and 1B, the device for implantation into the body may be in the form of an acetabular cup 10. The acetabular cup 10 preferably includes a metal insert 11 comprised of a bearing support structure 12, a bone ingrowth structure 14 and an intermediate structure 16. The acetabular cup 10 can be used in a total hip replacement surgery.


During the surgery, the joint of the hip, as shown in FIGS. 2 and 3, the hip socket 20 (acetabulum) and the ball 18 or head of the femur F are removed. An acetabular cup, such as acetabular cup 10, is positioned within the pelvis P. A first end 15 of a femoral stem FS is positioned within the femur F, while a second end 17, including a “ball” is positioned adjacent the bearing support structure 12 of the acetabular cup 10. Desirably, the second end 17 of the femoral stem FS is rotatably moveable relative to the acetabular cup 10.


The bone ingrowth structure 14, as well as the bearing support structure 12 and intermediate structure 16 of the acetabular cup 10 may be constructed using a direct laser remelt process as, for example, described in U.S. patent application Ser. No. 10/704,270, filed Nov. 7, 2003 entitled “Laser-Produced Porous Surface,” and U.S. patent application Ser. No. 11/027,421, filed Dec. 30, 2004, entitled “Laser-Produced Porous Structure,” the disclosures of which are hereby incorporated herein by reference.


As shown in FIG. 1A, in one preferred embodiment of the present invention, the bone ingrowth structure 14 is approximately 1.1 mm thick and has a porosity of approximately between the range of 70% to 80%. The intermediate structure 16 is approximately 0.1 mm thick and is substantially fully dense. The bearing support structure 12 is approximately 0.8 mm thick and is adapted for being secured within a polymer layer to form a bearing surface 8, as will be described below. The incorporation of the polymer, as described below, desirably results in an acetabular cup with a thickness of less than 4 mm, which is considered to be preferentially for resurfacing cups. The measurements are simply illustration and should not be considered a limitation since various thicknesses may be used when building the part.


The bone ingrowth structure 14 may be prepared by populating the volume of the structure with a single unit repeating cell using propriety software. A single unit cell 110 and the corresponding porous layer are shown in FIGS. 1C and 1D. The single cell 110 used is a unit cell octahedron structure having a length of 800 μm with vertical pillars on each corner. When tessellated, these cells produce porous structures having a porosity of approximately 80% with full interconnected porosity and mean pore sizes between 100 μm and 400 μm.


The intermediate structure 16 is designed to facilitate the bonding of the bearing support structure 12 to the bone ingrowth structure 12, as well as isolate the bone ingrowth structure from a polymeric material, as will be described below.


The bearing support structure 12 may be designed by populating the volume of the structure with a single repeating unit cell 112, as shown in FIGS. 1E and 1F. This produces a structure that is between 90% to 95% porous with fully interconnected porosity with pore sizes between 1.25 mm and 2 mm diameter. Of course, the dimension of the unit cell 112 may be altered or even a difference unit cell employed, such that the porosity of the structure may be customized based on desirability.


The porosity of each structure may be altered but in a preferred embodiment the porosity of each structure is dependent on that structures function. Thus the resultant porosity of the bone ingrowth structure 14 should be within a range that promotes bone ingrowth. The porosity of the bearing support structure 12 should be in a range that easily allows for a polymeric material or other material to adhere to the structure as will be described below. And the porosity of the intermediate layer should be in a range that prohibits or at least reduces the ability of a polymeric material to leech from the bearing support structure 12 to the bone ingrowth structure 14, as will be described below.


The files describing the bone ingrowth structure 14, solid intermediate structure 16 and the bearing support structure 12 may all be loaded into the operating software for a MCP realizer, FUSCO. The three structures are then reassembled and manufactured as one part. A schematic of the manufactured part and a photo of the final component are shown in FIG. 1G.


In one specific embodiment, the acetabular cup has a total thickness of 3 mm and an internal diameter of 46 mm.


According to one method of forming a porous three-dimensional structure by laser melting, a powder of titanium, titanium alloys, stainless steel, cobalt chrome alloys, tantalum or niobium is disposed onto a substrate. The laser melting process includes scanning a laser beam onto the powder and in parallel scan lines with a beam overlap, e.g., scan spacing, followed by similar additional scans or subsequent scans at 90 degrees, as way of example. The type of scan chosen may depend on the initial layer thickness as well as the web height required. The web height refers to the height of a single stage of the metal structure 11. The web height may be increased by depositing additional layers of powder of a structure and scanning the laser at the same angle of the previous scan. Further, the additional scan lines may be at any angle to the first scan, to form a structure with the formation of a defined porosity, which may be regular or random. The scanned device may be programmed to proceed in a random generated manner to produce an irregular porous construct but with a defined level of porosity. Furthermore, the scan can be preprogrammed using digitized images of various structures, such as the acetabular cup 10, shown in FIGS. 1A and 1B, to produce a similar structure. The scan may also be customized to a particular patient. In this process, a CT scan of for instance, a person's acetabulum is taken and inputted into a computer program. The resultant file may be sliced, digitized or manipulated by methods known to those in the art as well as described herein. Based on these files and tailored measurements, a customized implant may be fabricated for a particular individual.


To produce a bone ingrowth structure, such as the bone ingrowth structure 14 of the acetabular cup 10, the nature of the material formed as a result of laser melting of powder beads is principally dependent upon the thermal profile involved (heating rate, soaking time, cooling rate); the condition of the raw material (size and size distribution of powder particles); atmospheric conditions (reducing, inert or oxidizing chamber gas); and accurate control of the deposited layer thickness.


The most optimum porous structure for maximization of bone in-growth on a prosthesis has generally been found to be between approximately 60% to 80%. The preferred pore structure is irregular and interconnected, with a minimum pore size between about 80 μm and 100 μm and a maximum pore size between 80 μm and 800 μm.


The bone ingrowth structure 14, the bearing support structure 12 and the intermediate structure 16 of the acetabular cup 10 may be constructed using the apparatus shown in FIGS. 4 of 5. The apparatus of FIG. 4 may include an Nd; YAG industrial laser 30, integrated to an RSG 1014 analog galvo-scanning head 32 for providing a maximum scan speed of 500 mm per second. The laser beam 34 is directed into an atmospherically-controlled chamber 36, which consists of two computer-controlled platforms with powder delivery and part building. The powder is delivered from a variable capacity chamber 38 into the chamber 36 and is transported by a roller 40 to a build platform 42 above a variable capacity build chamber 44.


In one embodiment as shown in FIG. 4, the build and delivery system parameters are optimized for an even 100 μm coating of powder to be deposited for every build layer. For implant manufacture, the metals chosen as surface materials are all difficult to process due to their affinity for oxygen. Titanium and other alloys are easily oxidized when processed by laser in oxygen-containing atmosphere, their oxide products have high melting points and poor flowability. For this reason, and to prevent the formation of other undesirable phases, the methods may be carried out under an Argon inert atmosphere in chamber 36. Pressure may remain at or below atmospheric pressure during the entire application. In another example of forming a porous structure, a cobalt chrome alloy may be configured into square structures, called coupons. As shown in FIG. 6, an array of cobalt chrome coupons may be built onto a stainless steel substrate. The coupons were built as test subjects. The cobalt chrome alloy may have a particle size distribution of 90 less than 22 μm, i.e., 90% of the particles are less than 22 μm, the composition of which is shown in the table below.









TABLE 1







Composition of Co212-e CoCr alloy
















Element
Cr
Mo
Si
Fe
Mn
Ni
N
C
Co





Wt %
27.1
5.9
0.84
0.55
0.21
0.20
0.16
0.050
Balance









An array of nine sample coupons were produced as shown in FIG. 6, with the process of Table 2, using a maximum laser power of 78 watts (W) and laser scanning speed for each coupon varying between 100-260 mms-1. Of course a higher laser power may be employed; however, a higher laser power would also necessitate increasing the speed of the laser scan speed in order to produce the desired melting of the powder layer. A simple linear x-direction scan was used on each of the coupons. This allowed the processing parameter, beam overlap, to be used to control the space between successive scan lines. That is, with a 100 μm laser spot size, an overlap of −200% produces a 100 μm gap between scans. Although the acceptable range for the beam overlap is given at +50% to −1200% it should be duly noted that the negative number only refers to the fact the there is a gap as opposed to a beam overlap between successive scans. For instance a beam overlap of zero refers to the fact that successive scans on the same layer of powder border each other. A positive beam overlap produces more solid components in contrast to a more negative beam overlap, which produces a more porous structure. The less the beam overlap the more solid the resultant structure will be. In addition, a larger beam overlap may be used to create the attachment structure or bearing support structure 12, as compared to the intermediate structure 16. If the beam overlap was 5%, then 5% of the first scan is overlapped by the second scan. When computing the Andrew number the absolute value of the beam overlap is used. The complete set of process parameters used is shown in Table 2 below.









TABLE 2







Process parameters













Power
Layer
Beam
Scanning

No.
Overlap


Watts
Thickness
Diameter
Speed
Atmos-
of
(% of


(W)
(μm)
(μm)
(mms−1)
phere
Layers
line width)





78
100
100
100-260
No
16
25, 50, −500









The incremental changes in scanning speed and the size of the speed range were modified as the experiments progressed. To begin with, a large range of speeds was used to provide an initial indication of the material's performance and the propensity to melt. As the experiments progressed, the range was reduced to more closely define the process window. Speed and beam overlap variations were used to modify the specific energy density being applied to the powder bed and change the characteristics of the final structure. The complete series of parameters are given in FIG. 7, the parameters sets used for the definitive samples are shaded in gray.


The key laser parameters varied for forming the three-dimensional metallic porous structures are: (a) Laser scanning speed (v.) in (mms-1), which controls the rate at which the laser traverses the powder bed; (b) Laser power, P(W), which in conjunction with the laser spot size controls the intensity of the laser beam. The spot size was kept constant throughout the experiment; (c) Frequency, (Hz) or pulse repetition rate. This variable controls the number of laser pulses per second. A lower frequency delivers a higher peak power and vice versa.


The line width can be related to the laser scanning speed and the laser power to provide a measure of specific density, known as the “Andrew Number”, where:






An
=


P

b
×
v




(

J
/

mm

-
2



)







Where P denotes the power of the laser, v is the laser scanning speed and b denotes beam width of the laser. The Andrew number is the basis for the calculation of the present invention. The Andrew number may also be calculated by substituting the line separation (d) for beam width (b). The two methods of calculating the Andrew number will result in different values being obtained. When using line separation (d) as a factor only one track of fused powder is considered, whereas when using the beam width (b) as a factor, two tracks of fused powder are considered as well as the relative influence of one track to the next. For this reason we have chosen to concern ourselves with the Andrew number using scan spacing as a calculating factor. It can thus be appreciated, that the closer these tracks are together the greater the influence they have on one another.


Additionally, the laser power may be varied between 5 W and 1000 W. Utilizing lower power may be necessary for small and intricate parts but would be economically inefficient for such coatings and structures described herein. It should be noted that the upper limit of laser power is restricted because of the availability of current laser technology. However, if a laser was produced having a power in excess of 1000 W, the scanning speed of the laser could be increased in order that an acceptable Andrew number is achieved. A spot size having a range between 5 μm to 500 μm is also possible. For the spot size to increase while still maintaining an acceptable Andrew number, either the laser power must be increased or the scanning speed decreased.


The above formula gives an indication of how the physical parameters can vary the quantity of energy absorbed by the powder bed. That is, if the melted powder has limited cohesion, e.g. insufficient melting, the parameters can be varied to concentrate the energy supply to the powder. High Andrew numbers result in reduced pore coverage and an increase in pore size due to the effects of increased melt volume and flow. Low Andrew numbers result in low melt volume, high pore density and small pores. Current satisfactory Andrew numbers are approximately 0.3 J/mm-2 to 8 J/mm-2 and are applicable to many alternative laser sources. It is possible to use a higher powered laser with increased scanning speed and obtain an Andrew number within the working range stated above.


Line spacing or beam overlap can also be varied to allow for a gap between successive scan lines. It is, therefore, possible to heat selected areas. This gap would allow for a smaller or larger pore size to result. The best illustration of this is shown in FIGS. 8A to 8C where a −500% beam overlap has been applied. FIGS. 8A to 8C are scanning election microscope images of the surface structure of CoCr on stainless steel produced with a laser power of 82 W cw. FIG. 8A was produced with a laser scanning speed of 105 mms-1 and FIG. 8B was produced with a laser scanning speed of 135 mms-1 FIG. 8C is an image of the same structure in FIG. 8B, in section. There is a significant self-ordering within the overall structure. Larger columnar structures are selectively built leaving large regions of unmelted powder. It is worth noting that these pillars are around 300 μm wide, over 1.6 mm tall and fuse well with the substrate, as seen in FIG. 8C. Further analysis shows that the use of a hatched scanning format allows porosity to be more sufficiently controlled to allow the pore size to be directly controlled by the beam overlap.


The use of an optical inspection method to determine this approximate porosity is appropriate given the sample size. This method, although not accurate due to the filter selection process, can, if used carefully, provide an indication of porosity. This porosity level falls within the range of the desired porosity for bone ingrowth structures. The mechanical characteristics of the porous structures are determined by the extent of porosity and the interconnecting webs. A balance of these variables is necessary to achieve the mechanical properties required by the intended application.


Increased fusion may, if required, be obtained by heating the substrate, powder or both prior to scanning Such heating sources are commonly included in standard selective laser sintering/melting/remelting machines to permit this operation.


As described above, the process can be carried out on flat baseplates that provide for easy powder delivery in successive layers of around 100 μm thickness. Control of powder layer thickness is very important if consistent surface properties are required. The application of this technology can also be applied to curved surfaces such as those found in modern prosthetic devices such as acetabular cup 10, with refinements being made to the powder layer technique.


The structures may receive ultrasonic and aqueous cleaning. On close examination, the resultant porous surfaces produced by the Direct Laser Remelting process exhibit small particulates that are scattered throughout the structure. It is unclear at this stage whether these particulates are bonded to the surface or loosely attached but there are means to remove or consolidate the particulates if required, by for example acid etching, heat treatment, a combination of the two, or the like.


The Direct Laser Remelting process has the ability to produce porous structures that are suitable for bone in-growth applications. The powdered surfaces have undergone considerable thermal cycling culminating in rapid cooling rates that have produced very fine dendritic structures.


The Direct Laser Remelting process can produce effective bone in-growth surfaces and the manufacturing costs are reasonable.


In the preceding examples, the object has been to provide a metal insert having a porosity on a base but the present invention can also be used to provide a non-porous structure on such a base to form a three-dimensional structure. The same techniques can be utilized for the materials concerned but the laser processing parameters can be appropriately selected so that a substantially solid non-porous structure is achieved.


Again, a technique can be used to deposit the powder onto a suitable carrier, for example a mold, and to carry out the process without the use of a base so that a three-dimensional structure is achieved which can be either porous, as described above, or non-porous if required.


It will be appreciated that this method can, therefore, be used to produce article from the metals referred to which can be created to a desired shape and which may or may not require subsequent machining Yet again, such an article can be produced so that it has a graded porosity of, e.g., non-porous through various degrees of porosity to the outer surface layer. Such articles could be surgical prostheses, parts or any other article to which this method of production would be advantageous.


Although the porous structure has been discussed with regard to randomly depositing powder onto a substrate and selectively laser melting the powder while repeating layer after layer, in contrast, each layer or portion of a layer, may be scanned to create a portion of a plurality of predetermined unit cells. As successive layers of powder are deposited onto previous layers, the scanning and depositing of such layers continues the building process of a predetermined unit cell. When constructing the predetermined unit cells, the preferred embodiment includes employing a pulse high energy beam to form “spots” on the deposited powder layer. At least some of the “spots” are joined to produce struts or portions of struts, which constitute a portion of a predetermined unit cell. The spots may be created at random, in a continuous manner or a combination of the two. Examples of some possible geometric shapes of a unit cell are shown in FIGS. 9A-9D. As disclosed herein, by continuing the building process refers not only to a continuation of a unit cell from a previous layer but also a beginning of a new unit cell as well as the completion of a unit cell.


The invention can include a laser melting process that precludes the requirement for subsequent heat treatment of the structure, thereby preserving the initial mechanical properties of the core or base metal. The equipment used for the manufacture of such a device could be one of many currently available including the MCP Realiszer, the EOS M270, Trumpf Trumaform 250, the Arcam EBM S12 and the like. The laser may also be a custom produced laboratory device.


As shown in FIG. 5, one apparatus for constructing a structure comprised of predetermined unit cells may include a chamber 50 filled with an inactive gas such as argon and nitrogen. By using an inactive gas you can avoid oxidation of the metal powder 52. The three-dimensional model, such as metal insert 11 may be built on a base plate 51. The model is built in a layer by layer fashion.


As successive layers of metal powder are deposited onto previous layers, the laser head 53 projects a beam of energy 54 onto locations of the powder to thereby form a spot or portion of a strut of a predetermined unit cell. The laser scans the powder bed and projects the energy beam based on the slice data of the model contained in the computer program.


After a layer has been completed, successive layer of metal powder may be deposited onto the previous layer by the use of a powder feeder 55. The powder feeder 55 may work in conjunction with a piston 56 that is lowered prior to the depositing of the additional layer of metal powder. The piston 56 is desirably positioned under the substrate on which the metal structure is built. As each layer is processed, the piston 56 may be lowered and an additional layer of metal powder deposited onto the previous layer. In this manner, each layer of unprocessed powder is positioned at the same distance from the laser head 53. The laser beam is capable of being directed along a X, Y coordinate system such that the desired location of the layer of metal powder can be engaged by the beam of energy 54. The guiding of the laser beam is dependent on the manufacturing system used. For example, if an E-beam system is employed the movement of the E-beam is controlled by deployment of the magnetic fields. If a laser beam apparatus is employed, the movement or guidance of the laser beam is controlled by a galvanometer.


The pore density, pore size and pore size distribution can be controlled from one location on the structure to another. It is important to note that successive powder layers can differ in porosity by varying factors used for laser scanning powder layers. Additionally, the porosity of successive layers of powder can be varied by either creating a specific type of predetermined unit cell or manipulating various dimensions of a given predetermined unit cell.


As described in U.S. patent application Ser. No. 11/027,421, the disclosure of which is incorporated by reference herein, such unit cells designs can be a tetrahedron 60 (FIG. 9A), dodecahedron 62 (FIG. 9B), octahedron 64 (FIG. 9C), diamond, as well as many other various shapes. In addition, various struts may be removed from a unit cell to create an additional structure such as that shown in FIG. 9D. Besides regular geometric shapes as discussed above, the unit cells of the present invention may be configured to have irregular shapes where various sides and dimensions have little if any repeating sequences. The unit cells can be configured to build constructs that closely mimic the structure of trabecular bone for instance. Unit cells can be space filling, all the space within a three-dimensional object is filled with cells, or interconnected where there may be some space left between cells but the cells are connected together by their edges. The unit cells can also be constructed in a form of a lattice. Additionally, adjacent lattices may be isolated from one another or only partially attached.


The cells can be distributed within the construct a number of ways. Firstly, they may be made into a block within a computer added design (“CAD”) system where the dimensions correspond to the extent of the solid geometry. This block can then be intersected with the geometry representing the component to produce a porous cellular representation of the geometry. Secondly, the cells may be deformed so as to drape over an object thus allowing the cells to follow the surface of the geometry. Thirdly, the cells can be populated through the geometry following the contours of any selected surface.


The unit cell can be open or complete at the surface of the construct to produce a desired effect. For instance, open cells with truncated lattice struts produce a surface with a porosity and impart the surface with some degree of barb, whereas closed cells can be “peaky” so as to increase surface roughness.


Modifying the lattice strut dimensions can control the mechanical strength of the unit cell. This modification can be in a number of key areas. The lattice strut can be adjusted by careful selection of build parameters or specifically by changing the design of the cross-section of each strut. The density of the lattice can similarly be adjusted by modification of the density of the unit cells as can the extent and shape of porosity or a combination thereof. Clearly the overall design of the unit cell will also have a significant effect of the structural performance of the lattice. For instance, dodecahedral unit cells have a different mechanical performance when compared to a tetrahedral (diamond) structure.


As shown in FIG. 9A, in a tetrahedron 60, each point 70, 72, 74, and 76 is the same distance from the neighboring point. This structure is analogous to the arrangements of carbon atoms in diamond.


Each carbon atom in the diamond structure is surrounded by four nearest neighbors. They are connected together by bonds that separate them by a distance of 1.5445 angstroms. The angles between these bonds are 109.5 degrees. As a result, the central atom and its neighbors form a tetrahedron. This geometry as in the case discussed herein may then be scaled to appropriate value for the pore construct required.


The two key parameters used to define the relations regarding height, surface area, space height, volume of tetrahedron, and the dihedral angle of a tetrahedron are the strand length of the tetrahedron and, i.e., the diameter or height and width, cross section area of the strand i.e., strut. These two parameters control the pore size and porosity of the structure. The parameter editor and relation editor within a typical CAD system can be used to control these parameters. Hence, by changing the parameters one can change the fundamental properties of the porous structure. As shown in FIG. 9A, the diamond structure may have a circular cross-section strands or square cross-section strands. Although only two strand cross-sections are discussed herein, strands having various cross-sections are possible. Further, this is true with most of the designs for the unit cell.


To create the mesh as shown in FIG. 10, the unit cell can be instanced across the 3-D space to produce the required lattice. FIG. 11 illustrates a view of a diamond lattice structure with and without laser beam compensation. Laser beam compensation essentially allows the diameter of the beam to be taken into account. Without it the constructed geometry is one beam diameter too wide as the beam traces out the contour of the particular section being grown. When laser beam compensation is utilized, the contour is offset half a beam diameter all around the constructed geometry which is represented in the CAD file. Although various parameters may be used, the parameters employed to create the lattices of FIG. 11 include a laser power of 90.5 watts with an exposure time of 1,000 μsec from a point distance of 90 μm. Table 3 illustrates various other examples of parameters that may be used to create various unit cells.














TABLE 3






edge

laser

point



length
diameter
power
exposure
distance


Part build on SLM
μm
μm
Watts
μsec
μm







Diamond Structure
2000
200
90.5
1000
90


Diamond Structure
2000
200
90.5
1000
90


with compensation







Dodecahedron
1500
200
68.3
1000
90


Structure







Dodecahedron
1500
200
68.3
1000
90


Structure with







compensation







Modified
1500
200
90.5
1000
90


Truncated







Octahedron









As shown in FIGS. 9B and 12, the porous structure can also be created using a unit cell in the shape of a dodecahedron. The regular dodecahedron is a platonic solid composed of 20 polyhydron vertices, 30 polyhydron edges, and 12 pentagonal faces. This polyhydron is one of an order of five regular polyhedra, that is, they each represent the regular division of 3-dimensional space, equilaterally and equiangularly. This basic unit cell for a decahedron mesh can be built up in a CAD package using the following calculations and procedure. The dodecahedron has twelve regular pentagonal faces, twenty vertices, and thirty edges. These faces meet at each vertex. The calculations for a side length of a dodecahedron are given by simple trigonometry calculations and are known by those in the art.


In a method of use, a sweep feature is first used to model the dodecahedron structure by driving a profile along a trajectory curve. The trajectory curves are constructed from datum points corresponding to the vertices of the dodecahedron connected by datum curves. The type of profile remains constant along the sweep producing the model shown in FIG. 9B. The size and shape of the profile can be designed to suit the particular application and the required strut diameter. Once a particular unit cell has been designed, the cell can be instanced to produce a regular lattice as shown in FIG. 12. As a dodecahedron is not spaced filling, meshes are produced by simple offsetting of the unit cell and allowing some of the struts to overlap. This method of overlapping may be used with the alternate shapes of the unit cell.



FIG. 13 shows a view of a dodecahedron (with and without laser beam compensation, from left to right) structure using selective laser melting process parameters. Once again, although the parameters may be varied, the lattices of FIG. 13 were created using the following parameters; a laser power of 90.5 watts, exposure of the powder for 1,000 μsec and a point distance of 90 μm.


As shown in FIGS. 9C and 14, the unit cell of the present invention may also be constructed in the shape of a truncated octahedron. A truncated octahedron has eight regular hexagonal faces, six regular square faces, twenty-four vertices, and thirty-six edges. A square and two hexagons meet at each vertex. When the octahedron is truncated, it creates a square face replacing the vertex, and changes the triangular face to a hexagonal face. This solid contains six square faces and eight hexagonal faces. The square faces replace the vertices and thus this leads to the formation of the hexagonal faces. It should be noted here that these truncations are not regular polydra, but rather square-based prisms. All edges of an archamedian solid have the same length, since the features are regular polygons and the edges of a regular polygon have the same length. The neighbors of a polygon must have the same edge length, therefore also the neighbors and so on. As with previous unit cells, various dimensions such as the octahedron height, octahedron volume, octahedron surface area, octahedron dihydral angle, and truncated octahedron volume, truncated octahedron height, truncated octahedron area, truncated octahedron volume, truncated octahedron dihydral angle can be determined by simple trigonometry and are known by those skilled in the art.


In a method of use, a CAD model of the truncated octahedron is constructed using the sweep feature and calculations and dimensions are incorporated using basic trigonometry. To tessellate the unit cell, the unit cell is first reoriented to enable easy tessellation and to reduce the number of horizontal struts in the model. Further, the model can be modified to remove all of the horizontal struts as shown in FIG. 9D. The modified structure is reproduced in order to save file size in the Steriolithography (“STL”) format of the program. Next, in order to create the unit cells, the method of using a laser melting process is performed. In one preferred embodiment, the parameter chosen includes a laser power of 90.5 watts, an exposure of 1000 μsec with a point distance of 90 μm. FIG. 8B illustrates a lattice structure formed using a plurality of individual truncated octahedron. As discussed earlier, the removal of various struts can create a barb effect on the exterior surface of the lattice structure.


As shown in FIGS. 15A-D, it is possible to reduce the size of the unit cell geometry. Also as shown, it is possible to manufacture open cell structures with unit cell sizes below 1 millimeter. FIG. 15A illustrates truncated octahedron structures manufactured using the laser melting process. All the structures were created using a laser power of 90.5 W, and a point distance of 90 μm; however, from left to right, the exposure time was varied from 500 μsec and 100 μsec. FIG. 15 illustrates similar structures and parameters as used with FIG. 15A, however, the unit cell used to create the lattice is diamond. FIGS. 9C and 9D illustrate a side view of the truncated octahedron structure of FIG. 15A and the diamond structure of FIG. 15B, respectively. Table 4 includes various manufacturing parameters used to construct various unit cell structure.















TABLE 4





Part





Point


build
Strand
Length of
Width of
Laser
Expo-
dis-


on
length
strand c/s
strand c/s
Power
sure
tance


SLM
μm
μm
μm
Watts
μsec
μm





















Truncated
3000
50
50
90.5
500
90


Octahedron








Truncated
3000
50
50
90.5
300
90


Octahedron








Truncated
3000
50
50
90.5
100
90


Octahedron








Truncated
1000
50
50
90.5
500
90


Octahedron








Truncated
1000
50
50
90.5
300
90


Octahedron








Truncated
1000
50
50
90.5
100
90


Octahedron








Diamond
700
50
50
90.5
500
90


Structure








Diamond
700
50
50
90.5
300
90


Structure








Diamond
700
50
50
90.5
100
90


Structure










Pseudorandom representative geometries may be made from the current regular unit cells by applying a random X, Y, Z perturbation to the vertices of the unit cells. One such example can be seen in FIG. 16. In another aspect of the present invention, various freestanding constructs can be generated.


Various other methods may also be utilized to produce the bone ingrowth structure 14, bearing support structure 12 and/or the intermediate structure 16 of the acetabular cup 10 in methods known to those in the art.


In one preferred embodiment, the average pore size of the bone ingrowth structure 14 falls within 280 μm to 480 μm, as measured using conventional linear intercept methods. A bimodal pore size distribution may be present as, for example, small pores within a 250 μm to 450 μm range and larger pores within a 600 μm to 800 μm range. The metal insert 11, i.e., the bone ingrowth structure 14, the bearing support structure and the intermediate structure 14 may be isotropic as, for example, without directionality with regard to the structure, and mechanical properties.


In one preferred embodiment, the average pore sizes of the porous layer 14 for interconnecting pores exceeds 250 μm with at least 99% and the pore volume therefore within between 65% to 75% of interconnecting pores exceeding 180 μm.


The general thickness of the porous layer generally lies within the range of between 1 mm to 2 mm but may be larger or smaller if so required.


The porous structure 14, bearing support structure 12 and the intermediate structure 16 may be formed simultaneously using any of the processes described herein or a combination of the processes.


Once the metallic structure has been formed, e.g., the bone ingrowth, bearing and intermediate structures, a polymeric material may be connected to the bearing support structure 12 to enable the acetabular cup 10 to bear against an articulating surface of an additional element. The polymeric material will comprise the bearing surface 8 of the acetabular cup 10


Depending on the material used to create the bearing surface 8, the polymeric material can be integrated with the bearing support structure 12, by compression molding, injection molding or heat forming. It may also be possible to cast certain types of materials from solution as, for example, polyurethane.


If the polymeric material used to form the bearing surface 8 is an ultra-high molecular weight polyethylene (“UHMWPE”) material or the like, the metallic insert, i.e., the bone ingrowth structure 14, the bearing support structure 12 and the intermediate structure 16, but specifically the bearing support structure 12, may be joined to the bearing surface 8 by a compression molding process using a matched metal die. The metal insert 11 is placed into a cavity part of a metal die. The polymer powder may then be added to the cavity of the metal die and desirably is dispersed against the bearing support structure 12. The cavity of the metal die is sealed and the metal die is then heated to a required temperature. As the temperature of the polymer powder is increased, the polymer powder begins to soften or melt so as to be flowable. Increased pressure onto the polymer powder may also aid in the melting process. Fusion of the polymer powder and attachment to the bearing support structure 12 is achieved when the acquired application of heat and pressure is reached. Subsequent cooling under pressure allows solidification of the polymer powder, which thus forms the bearing surface 8 that is securely attached to the bearing support structure 12. A final machining operation may be required to complete the construct of the bearing surface 8.


In one preferred embodiment, the metal insert 11 is situated in the metal die with the bone ingrowth structure 14 bounded within the cavity of the metal die such that the polymer material cannot come in contact with the bone ingrowth structure. And since the intermediate structure 16 is preferably substantially solid, the intermediate structure prohibits or at least, reduces the ability of the polymeric material to come in contact with the bone ingrowth structure as the polymeric material attaches to the bearing support structure 12 to form a bearing surface 8. By keeping the pores of the bone ingrowth structure unencumbered with polymer material, the ability of the bone ingrowth structure to promote bone ingrowth is not altered.


In an alternate embodiment, an injection molding process may be carried out in order to fuse the bearing surface 8 to the bearing support structure 12. An injection molding process may be preferred when the material used to create the bearing surface 8 is a polyurethane or chopped-fiber-reinforced poly (ETHERETHERKETONE) (“CFRPEEK”). Similar to the compression molding process, in the injection molding process, the metal insert 11 is secured into a cavity of an injection molding machine and the mold closed. As with the previous embodiment, the bone ingrowth structure 14 may be isolated from the polyurethane or additional polymer used. The selected material, e.g., polyurethane or CFRPEEK is heated in a barrel of the injection molding machine. Once the selected material is heated in the barrel of the injection mold, the pressure may be applied to the selected material to urge the heated selected material from the barrel into the mold cavity and onto a surface of the bearing support structure 12. Upon cooling, the selected material is fused to the bearing support structure 12 so as to form the bearing surface 8 upon which the acetabular cup 10 may move relative to an additional element, i.e., the femoral stem FS. Upon cooling, the completed part may be removed from the injection mold and machined if so required. The mold cavity can be configured such that particular features, designs and contours of the bearing surface 8 may be formed.


In still yet another alternate embodiment, the bearing surface 8 may be formed using a heat forming process. In a heat-forming process, materials such as UHMWPE are supplied as fabricated rod stock suitable for machining. Profiles can be produced by machining the fabricated rod stock to represent a near net shape of the intended article such as the bearing surface 8 of the acetabular cup 10. Once the article has been produced, both the metal insert 11 and the shape polymer machine part are placed into a mold and heated to the required temperature. Upon the application of heat and pressure, the softened polymer is forced into and against the metal insert 11, specifically the bearing support structure 12. Upon cooling, solidification takes place and the polymer is secured to the metal insert 11 and specifically the bearing support structure 12. Further machining may be required if necessary once the part has been allowed to cool and is removed from the mold.


As with previous embodiments, in combination with the intermediate structure 16 and additional elements, the bone ingrowth structure 14 may be isolated from any polymeric material so that the polymeric material cannot affect the ability of the structure to promote bone ingrowth.


In yet still another alternate embodiment, the bearing surface 8 may be constructed using a solution casting method. In a solution casting method, a material, such as a polyurethane material, can be formed by casting solvent-dissolved solutions in the mold.


In addition to the method as described above, it is also possible to make the bearing surface 8 out of additional material such as a metallic material or ceramic material. As such, when forming the bearing surface 8 from a metallic material, the selective laser melting process, described herein, as well as in U.S. patent application Ser. Nos. 10/704,270, and 11/027,421 (described above) may be utilized.


An example of a process for forming the acetabular cup 10 is discussed herein, although various methods may be employed. In a preferred method, software and equipment, as shown in Table 6 below, may be employed to build a finished product.










TABLE 6





Equipment/Software
Description







MCP realiser
SLM machine using 100 w fibre laser


Magics V8.05 (Materialise)
CAD software package used for



manipulating STL files and preparing



builds for Rapid Manufacture (RM)


Manipulator 3.4.1
Propriety program for populating a



solid STL file with porous surface



coating. Outputs a sliced F&S file



ready for manufacture


Fusco
MCP realiser operating software


Gas atomized co - titanium powder
Metal powder with a mean particle



size of approximately 40 μm









In a first step of such process, a CAD file of an acetabular cup component is loaded into the Magics software package as a single part, as shown in FIG. 17. The file may then be divided into three separate solid volumes having a 1.1 mm thick outer layer—this layer will be used to create the 80% porous bone ingrowth surface; 0.1 mm thick intermediate layer—this layer will be a fully dense layer that supports the bone ingrowth surface; and 0.8 mm thick inner layer—this will be used to create an interlock surface for a polymer injection molding. The three layers, when completed, will comprise the metal insert 11 of the acetabular cup 10.


A completed acetabular cup 10 is shown is shown in FIG. 17 and includes a bearing surface 8, an intermediate structure 16 and a bone ingrowth structure 12. The bone ingrowth structure 14 may include fins or protrusions 13 for anchoring into bone.


In an alternate embodiment of the present invention, the acetabular cup may be constructed with a two tier structure. As shown in FIG. 18, which is a cross section of an acetabular cup 110, the two tier structure includes a metal insert 111 having a bone ingrowth structure 114 and a bearing support structure 112. The bearing surface 108 is attached to the bearing support structure 112 are connected directly to one another. But each structure is adapted for its own purpose, i.e., the bone ingrowth structure 14 has a porosity adapted for bone ingrowth and the bearing support structure 12 has a porosity suited for anchoring a polymeric material or additional material as discussed herein.


Although, the figure illustrates a demarcation between the two structures, highlighting the difference in porosity between the two, the actual metal insert 111 may have a graded porosity which increases, decreases or some combination of the two along an axis 119 passing through the center of the acetabular cup 110.


In yet another alternate embodiment, as shown in FIG. 19, the acetabular cup 210 may have a plurality of structures comprising a metal insert 211. The metal insert 211 may include a bone ingrowth structure 214, an intermediate structure 216 and a bearing support structure 212. The intermediate structure 216 may include a first barrier 217, a second barrier 218 and a bridging structure 219. The first barrier 217 and second barrier 218 may be substantially solid while the bridging structure 219, positioned between the two barriers has a particular porosity. The particular porosity may be specifically designed to transfer mechanical loads through the overall construct to a bone to which the acetabular cup is attached to. Once the metal insert 211 is designed, the bearing surface 208 may be coupled thereto as described herein.


Although the present invention has been discussed with regard to constructing an acetabular cup, various other orthopedic implants, tools, apparatus, and structures may also be built using the same process. For instance, a patella component 300, as shown in FIGS. 20 and 21, includes a baseplate 302 and a bearing surface 304.


As with the acetabular cup discussed herein, once the baseplate 302 had been constructed, the patella bearing surface 304 may be attached to the baseplate 302 using the processes discussed herein.


In a method of assembly, the patella is shaved on a posterior side to a desired depth and some of the cartilage surrounding the area is removed. The baseplate 302 of the patella component preferably includes a plurality of pegs 306 that engage the remaining bone of the patella. The pegs 306 are designed for bone ingrowth as discussed in here. With the pegs 306 attached to the posterior of the patella, the bearing surface 304 may replace and perform the function of any cartilage removed from the area.


In yet another alternate embodiment, as shown in FIGS. 22 and 23, the present invention can be used to construct a cartilage plug 400. The cartilage plug 400 desirably includes a metal insert 401 having a bone ingrowth structure 402, an intermediate structure 403 and a bearing support structure 404. The metal insert 401 may be constructed using methods discussed herein. Once the metal insert 401 is completed, the bearing surface 408 may be attached to the bearing support structure 404 as discussed herein.


For illustration purposes, the bearing support structure 404 is comprised of two independent lattices 406 and 407. The lattices 406 and 407 are independent from one another and may be constructed differently from each other. In alternate embodiments, the bearing support structure 404 may be constructed similar to the bearing support structure 12 of the metal insert 11, discussed herein.


The cartilage plug 400 may be employed as for example when only a portion of a tibial plateau must be replaced. A bore is created in the tibial plateau removing the defective portion and than filled with the cartilage plug 400. The bone ingrowth structure 514 of the cartilage plug 400 is positioned within the bone while the bearing surface 408 faces outward to replace any cartilage removed from the area.


In yet another alternate embodiment not shown in the figures, the intermediate structure of an implant may be constructed using a die cast or any method known to those in the art. The resultant intermediate structure may then be placed onto the base plate of an apparatus similar to that shown in FIG. 4 or 5. Once in place, a bone ingrowth structure and bearing support structure may be built onto the intermediate structure.


As previously discussed, a bearing surface may be attached to an implant or metal insert indirectly. For example, as shown in FIG. 24, a metal insert 511 may be constructed similar to metal insert 11 in the shape of an acetabular cup 510, and include a bone ingrowth structure 514, an intermediate structure 516 and a bearing support structure 512. A bone cement 506 may be deposited and attached to the bearing support structure 512, in methods known to those in the art. A UHMWPE liner 509 is positioned adjacent the bone cement and is subsequently attached thereto as the bone cement polymerizes. The liner 509 preferably includes an exterior 502 and an interior 503. The exterior 502 of the liner 509 preferably includes a plurality of attachment sites such as radial grooves or as shown in the figure, circumferential grooves 504. As the liner 509 is forced against the bone cement the bone cement engages the grooves. As the bone cement 506 polymerizes, the liner 509 is mechanically interlocked to the bone cement.


The interior 503 of the liner 509 is suitable to act as a bearing surface of the completed acetabular cup 510. Preferably, the metal insert 511 and liner 509 are prepackaged and available to a surgeon in a plurality of sizes such that during surgery the surgeon only has to remove the desired liner and insert once the specific measurements and requirements have been decided upon.


Systems incorporating the used of a liner cemented to a porous metal insert are normally used when the acetabulum has been severely damaged or in some cases of revision surgery.


Although not shown in the figures, the present invention may be in the shape of a glenoid or any other component where bone ingrowth is desired in combination with a bearing surface.


As with all of the embodiments herein, it is possible to apply a coating of a bone growth enhancer as, for example, hydroxyapatite, bonemorphogenic protein such as OP-1 (Stryker), to the surface intended to be in direct contact with bone.


Although the invention herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present invention. It is therefore to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the present invention as defined by the appended claims.

Claims
  • 1. An orthopedic implant comprising: porous first and second structures separated from each other, at least a portion of either one or both of the first and second structures being defined by tessellated cells, each cell being formed of struts including a first plurality of struts defining a first plane and a second plurality of struts sharing a strut with the first plurality of struts and defining a second plane transverse to the first plane; andan intermediate structure directly attached to the first and the second structures, the intermediate structure having a different porosity than the first and the second structures.
  • 2. The orthopedic implant of claim 1, wherein a porosity of the first structure is different than a porosity of the second structure.
  • 3. The orthopedic implant of claim 1, wherein the first structure and the second structure are metallic.
  • 4. The orthopedic implant of claim 1, wherein the first structure is a bone ingrowth structure and the second structure is a bearing support structure.
  • 5. The orthopedic implant of claim 4, further comprising a polymeric bearing surface interlocked with the bearing support structure, wherein the intermediate structure inhibits the polymeric material from translating through the bearing support structure to the bone ingrowth structure.
  • 6. The orthopedic implant of claim 1, wherein the intermediate structure includes an entire layer that is substantially solid.
  • 7. The orthopedic implant of claim 1, wherein an entirety of the intermediate structure is located between the first and the second structures.
  • 8. The orthopedic implant of claim 1, wherein the cells are polyhedral unit cells.
  • 9. The orthopedic implant of claim 1, wherein the first structure is a bone ingrowth structure having pores with diameters in a range of 80 μm to 800 μm.
  • 10. The orthopedic implant of claim 9, wherein the second structure has pores with diameters exceeding 800 μm.
  • 11. The orthopedic implant of claim 1, wherein the cells define polygons.
  • 12. The orthopedic implant of claim 1, wherein the cells define irregular polygons.
  • 13. The orthopedic implant of claim 1, wherein the orthopedic implant includes multiple gradient porosities.
  • 14. The orthopedic implant of claim 1, wherein the cells define polygons and the first structure is a bone ingrowth structure having pores with diameters in the range of 80 inn to 800 μm.
  • 15. The orthopedic implant of claim 1, wherein the tessellated cells of the first and second structures have irregular shapes.
  • 16. The orthopedic implant of claim 1, wherein the tessellated cells have a tetrahedron, dodecahedron, octahedron, or diamond shape.
  • 17. An orthopedic implant comprising: porous metallic first and second structures separated from each other, at least a portion of either one or both of the first and second structures being defined by tessellated cells; anda solid intermediate structure directly attached to each of the first and the second structures,wherein the cells define polygons andwherein the first structure has pores with diameters in the range of 80 μm to 800 μm and the second structure has pores with diameters exceeding 800 μm.
CROSS-REFERENCE TO RELATED APPLICATION

The present application is a continuation of U.S. patent application Ser. No. 15/788,304 filed Oct. 19, 2017, which is a continuation of U.S. patent application Ser. No. 14/276,483 filed May 13, 2014, now U.S. Pat. No. 10,398,559, which is a continuation of U.S. patent application Ser. No. 11/295,008 filed Dec. 6, 2005, now U.S. Pat. No. 8,728,387, the disclosures of which are hereby incorporated herein by reference.

US Referenced Citations (415)
Number Name Date Kind
14403 Brown et al. Mar 1856 A
222687 Fresco Dec 1879 A
2373769 Macy Apr 1945 A
3520099 Mattes Jul 1970 A
3556918 Lemelson Jan 1971 A
3605123 Pratt et al. Sep 1971 A
3806961 Muller Apr 1974 A
3816855 Saleh Jun 1974 A
3826054 Culpepper, Jr. Jul 1974 A
3906550 Rostoker et al. Sep 1975 A
4047349 Aguilar, Jr. Sep 1977 A
4073999 Bryan et al. Feb 1978 A
4085466 Goodfellow et al. Apr 1978 A
4117302 Earle et al. Sep 1978 A
4154040 Pace May 1979 A
4164794 Spector et al. Aug 1979 A
4179485 Tritten Dec 1979 A
4202055 Reiner et al. May 1980 A
4218494 Belmondo et al. Aug 1980 A
4247508 Housholder Jan 1981 A
4259072 Hirabayashi et al. Mar 1981 A
4305340 Iwaki et al. Dec 1981 A
4344193 Kenny Aug 1982 A
4385404 Sully et al. May 1983 A
4444818 Tominaga et al. Apr 1984 A
4474861 Ecer Oct 1984 A
4479271 Bolesky et al. Oct 1984 A
4502161 Wall Mar 1985 A
4513045 Bondoc et al. Apr 1985 A
4542539 Rowe, Jr. et al. Sep 1985 A
4543158 Bondoc et al. Sep 1985 A
4550448 Kenna Nov 1985 A
4636219 Pratt et al. Jan 1987 A
4644942 Sump Feb 1987 A
4673408 Grobbelaar Jun 1987 A
4673409 Van Kampen Jun 1987 A
4714473 Bloebaum Dec 1987 A
4714474 Brooks, Jr. et al. Dec 1987 A
4719908 Averill et al. Jan 1988 A
4766029 Brock et al. Aug 1988 A
4863538 Deckard Sep 1989 A
4944756 Kenna Jul 1990 A
4944817 Bourell et al. Jul 1990 A
4957819 Kawahara et al. Sep 1990 A
4961154 Pomerantz et al. Oct 1990 A
4969302 Coggan et al. Nov 1990 A
4969907 Koch et al. Nov 1990 A
4969910 Frey et al. Nov 1990 A
4976738 Frey et al. Dec 1990 A
4978355 Frey et al. Dec 1990 A
4990163 Ducheyne et al. Feb 1991 A
4997445 Hodorek Mar 1991 A
5002572 Picha Mar 1991 A
5004476 Cook Apr 1991 A
5017753 Deckard May 1991 A
5024670 Smith et al. Jun 1991 A
5031120 Pomerantz et al. Jul 1991 A
5034186 Shimamune et al. Jul 1991 A
5053090 Beaman et al. Oct 1991 A
5067964 Richmond et al. Nov 1991 A
5076869 Bourell et al. Dec 1991 A
5080674 Jacobs et al. Jan 1992 A
5090174 Fragale Feb 1992 A
5108432 Gustavson Apr 1992 A
5108441 McDowell Apr 1992 A
5147402 Bohler et al. Sep 1992 A
5150304 Berchem et al. Sep 1992 A
5155324 Deckard et al. Oct 1992 A
5158574 Stone Oct 1992 A
5171282 Pequignot Dec 1992 A
5176710 Hahn et al. Jan 1993 A
5192328 Winters Mar 1993 A
5219362 Tuke et al. Jun 1993 A
5274565 Reuben Dec 1993 A
5282861 Kaplan Feb 1994 A
5282870 Moser et al. Feb 1994 A
5287435 Cohen et al. Feb 1994 A
5314478 Oka et al. May 1994 A
5323954 Shetty et al. Jun 1994 A
5336518 Narayanan et al. Aug 1994 A
5352405 Beaman et al. Oct 1994 A
5356433 Rowland et al. Oct 1994 A
5358529 Davidson Oct 1994 A
5368602 de la Torre Nov 1994 A
5370692 Fink et al. Dec 1994 A
5386500 Pomerantz et al. Jan 1995 A
5397359 Mittelmeier et al. Mar 1995 A
5398193 deAngelis Mar 1995 A
5425210 Zafir Jun 1995 A
5443510 Shetty et al. Aug 1995 A
5443518 Insall Aug 1995 A
5461839 Beck Oct 1995 A
5486599 Saunders et al. Jan 1996 A
5489306 Gorski Feb 1996 A
5490962 Cima et al. Feb 1996 A
5496372 Hamamoto et al. Mar 1996 A
5504300 Devanathan et al. Apr 1996 A
5507815 Wagner et al. Apr 1996 A
5510066 Fink et al. Apr 1996 A
5514183 Epstein et al. May 1996 A
5518680 Cima et al. May 1996 A
5526627 Beck Jun 1996 A
5549700 Graham et al. Aug 1996 A
5571185 Schug Nov 1996 A
5571196 Stein Nov 1996 A
5580353 Mendes et al. Dec 1996 A
5609646 Field et al. Mar 1997 A
5616294 Deckard Apr 1997 A
5624463 Stone et al. Apr 1997 A
5632745 Schwartz May 1997 A
5640667 Freitag et al. Jun 1997 A
5648450 Dickens, Jr. et al. Jul 1997 A
5665118 LaSalle et al. Sep 1997 A
5681354 Eckhoff Oct 1997 A
5702448 Buechel et al. Dec 1997 A
5714103 Bauer et al. Feb 1998 A
5728162 Eckhoff Mar 1998 A
5729946 Beck Mar 1998 A
5735903 Li et al. Apr 1998 A
5749874 Schwartz May 1998 A
5768134 Swaelens et al. Jun 1998 A
5769092 Williamson, Jr. Jun 1998 A
5769899 Schwartz et al. Jun 1998 A
5773789 Devanathan et al. Jun 1998 A
5776201 Colleran et al. Jul 1998 A
5782908 Cahalan et al. Jul 1998 A
5795353 Felt Aug 1998 A
5798924 Eufinger et al. Aug 1998 A
5824098 Stein Oct 1998 A
5824102 Buscayret Oct 1998 A
5839247 Beck Nov 1998 A
5857303 Beck et al. Jan 1999 A
5866113 Hendriks et al. Feb 1999 A
5879387 Jones et al. Mar 1999 A
5879398 Swarts et al. Mar 1999 A
5928285 Bigliani et al. Jul 1999 A
5973222 Devanathan et al. Oct 1999 A
5987838 Beck Nov 1999 A
5989472 Ashby et al. Nov 1999 A
6013855 McPherson et al. Jan 2000 A
6042774 Wilkening et al. Mar 2000 A
6045581 Burkinshaw Apr 2000 A
6046426 Jeantette et al. Apr 2000 A
6049054 Panchison et al. Apr 2000 A
6077989 Kandel et al. Jun 2000 A
6087553 Cohen et al. Jul 2000 A
6096043 Techiera et al. Aug 2000 A
6112109 D'Urso Aug 2000 A
6128866 Wearne Oct 2000 A
6132468 Mansmann Oct 2000 A
6139585 Li Oct 2000 A
6149688 Brosnahan et al. Nov 2000 A
6164032 Beck Dec 2000 A
6171340 McDowell Jan 2001 B1
6190407 Ogle et al. Feb 2001 B1
6206924 Timm Mar 2001 B1
6206927 Fell et al. Mar 2001 B1
6209621 Treacy Apr 2001 B1
6215093 Meiners et al. Apr 2001 B1
6217615 Sioshansi et al. Apr 2001 B1
6248131 Felt et al. Jun 2001 B1
6251143 Schwartz et al. Jun 2001 B1
6254639 Peckitt Jul 2001 B1
6261322 Despres, III et al. Jul 2001 B1
6261493 Gaylo et al. Jul 2001 B1
6280478 Richter et al. Aug 2001 B1
6283997 Garg et al. Sep 2001 B1
6290726 Pope et al. Sep 2001 B1
6299645 Ogden Oct 2001 B1
6344061 Leitao et al. Feb 2002 B1
6350284 Tormala et al. Feb 2002 B1
6355086 Brown et al. Mar 2002 B2
6368354 Burstein et al. Apr 2002 B2
6370382 Kang et al. Apr 2002 B1
6371958 Overaker Apr 2002 B1
6379816 De Loose et al. Apr 2002 B1
6385585 Jonsson et al. May 2002 B1
6395327 Shetty May 2002 B1
6406497 Takei Jun 2002 B2
6415574 Beck Jul 2002 B2
6454811 Sherwood et al. Sep 2002 B1
6476343 Keicher et al. Nov 2002 B2
6482209 Engh et al. Nov 2002 B1
6494914 Brown et al. Dec 2002 B2
6520996 Manasas et al. Feb 2003 B1
6530951 Bates et al. Mar 2003 B1
6551608 Yao Apr 2003 B2
6558421 Fell et al. May 2003 B1
6582715 Barry et al. Jun 2003 B1
6589283 Metzger et al. Jul 2003 B1
6592598 Vibe-Hansen et al. Jul 2003 B2
6599301 Vibe-Hansen et al. Jul 2003 B2
6599322 Amrich et al. Jul 2003 B1
6599323 Melican et al. Jul 2003 B2
6610067 Tallarida et al. Aug 2003 B2
6626945 Simon et al. Sep 2003 B2
6632246 Simon et al. Oct 2003 B1
6652246 Lin et al. Nov 2003 B1
6652587 Felt et al. Nov 2003 B2
6676892 Das et al. Jan 2004 B2
6679917 Ek Jan 2004 B2
6682567 Schroeder Jan 2004 B1
6686437 Buchman et al. Feb 2004 B2
6699252 Farr, II et al. Mar 2004 B2
6702848 Zilla et al. Mar 2004 B1
6709462 Hanssen Mar 2004 B2
6712822 Re et al. Mar 2004 B2
6712856 Carignan et al. Mar 2004 B1
6716957 Tunc Apr 2004 B2
6743232 Overaker et al. Jun 2004 B2
6770099 Andriacchi et al. Aug 2004 B2
6772026 Bradbury et al. Aug 2004 B2
6802864 Tornier Oct 2004 B2
6811569 Afriat et al. Nov 2004 B1
6843807 Boyce Jan 2005 B1
6846329 McMinn Jan 2005 B2
6850125 Norman et al. Feb 2005 B2
6852125 Simon et al. Feb 2005 B2
6855165 Fell et al. Feb 2005 B2
6863689 Ralph et al. Mar 2005 B2
6866684 Fell et al. Mar 2005 B2
6893463 Fell et al. May 2005 B2
6911044 Fell et al. Jun 2005 B2
6916341 Rolston Jul 2005 B2
6921264 Mayer et al. Jul 2005 B2
6923831 Fell et al. Aug 2005 B2
6932610 Ono et al. Aug 2005 B2
6966932 Schroeder Nov 2005 B1
6993406 Cesarano, III et al. Jan 2006 B1
7051417 Michelson May 2006 B2
7168283 Van Note et al. Jan 2007 B2
7332537 Bredt et al. Feb 2008 B2
7465318 Sennett et al. Dec 2008 B2
7494507 Dixon et al. Feb 2009 B2
7497876 Tuke et al. Mar 2009 B2
7521017 Kunze et al. Apr 2009 B2
7563284 Coppes et al. Jul 2009 B2
7597715 Brown et al. Oct 2009 B2
7632575 Justin et al. Dec 2009 B2
7655047 Swords Feb 2010 B2
7674517 Ramsey et al. Mar 2010 B2
7718109 Robb et al. May 2010 B2
7747305 Dean et al. Jun 2010 B2
7779890 Frasier et al. Aug 2010 B2
7875083 Sudmann Jan 2011 B2
7879275 Smith et al. Feb 2011 B2
7922765 Reiley Apr 2011 B2
7931931 Yan Apr 2011 B2
8029575 Borden Oct 2011 B2
8066770 Rivard et al. Nov 2011 B2
8090540 Leo et al. Jan 2012 B2
8247333 Sypeck et al. Aug 2012 B2
8292967 Brown et al. Oct 2012 B2
8308807 Seebeck et al. Nov 2012 B2
8350186 Jones et al. Jan 2013 B2
8414648 Reiley Apr 2013 B2
8551173 Lechmann et al. Oct 2013 B2
8734462 Reiley et al. May 2014 B2
8796015 Gingras Aug 2014 B2
8843229 Vanasse et al. Sep 2014 B2
8864826 Pressacco Oct 2014 B2
8979938 Linares Mar 2015 B2
8985430 Charlebois et al. Mar 2015 B2
8992703 O'Neill Mar 2015 B2
9370426 Gabbrielli et al. Jun 2016 B2
9375323 Reiley Jun 2016 B2
9486264 Reiley et al. Nov 2016 B2
9801974 Landon Oct 2017 B2
9949843 Reiley et al. Apr 2018 B2
10045854 Adams Aug 2018 B2
10398559 Jones Sep 2019 B2
10744426 Glover Aug 2020 B2
10806557 Chen Oct 2020 B1
11155073 O'Neill Oct 2021 B2
11186077 O'Neill Nov 2021 B2
11510783 O'Neill et al. Nov 2022 B2
20010014403 Brown et al. Aug 2001 A1
20020007294 Bradbury et al. Jan 2002 A1
20020010512 Takei Jan 2002 A1
20020015654 Das et al. Feb 2002 A1
20020016635 Despres et al. Feb 2002 A1
20020062154 Ayers May 2002 A1
20020102674 Anderson Aug 2002 A1
20020127328 Shetty Sep 2002 A1
20020130112 Manasas et al. Sep 2002 A1
20020151983 Shetty Oct 2002 A1
20020173855 Mansmann Nov 2002 A1
20020187458 Dolabdjian et al. Dec 2002 A1
20020198528 Engh et al. Dec 2002 A1
20030012805 Chen et al. Jan 2003 A1
20030032351 Horner et al. Feb 2003 A1
20030033018 Merchant Feb 2003 A1
20030045941 Lewallen Mar 2003 A1
20030055500 Fell et al. Mar 2003 A1
20030055501 Fell et al. Mar 2003 A1
20030060882 Fell et al. Mar 2003 A1
20030060883 Fell et al. Mar 2003 A1
20030060884 Fell et al. Mar 2003 A1
20030060885 Fell et al. Mar 2003 A1
20030060888 Fell et al. Mar 2003 A1
20030065400 Beam et al. Apr 2003 A1
20030069638 Barlow et al. Apr 2003 A1
20030069718 Hollister et al. Apr 2003 A1
20030153977 Suguro et al. Aug 2003 A1
20030153981 Wang Aug 2003 A1
20030155686 Hawkins et al. Aug 2003 A1
20030158606 Coon et al. Aug 2003 A1
20030206820 Keicher et al. Nov 2003 A1
20030209305 Smith et al. Nov 2003 A1
20030220696 Levine et al. Nov 2003 A1
20040006393 Burkinshaw Jan 2004 A1
20040009228 Tormala et al. Jan 2004 A1
20040015170 Tallarida et al. Jan 2004 A1
20040023586 Tilton Feb 2004 A1
20040044414 Nowakowski Mar 2004 A1
20040054416 Wyss et al. Mar 2004 A1
20040059356 Gingras Mar 2004 A1
20040098132 Andriacchi et al. May 2004 A1
20040121110 Schmidt et al. Jun 2004 A1
20040143339 Axelson et al. Jul 2004 A1
20040143341 McLean Jul 2004 A1
20040148030 Ek Jul 2004 A1
20040153163 Posner Aug 2004 A1
20040162622 Simon et al. Aug 2004 A1
20040167633 Wen et al. Aug 2004 A1
20040191106 O'Neill Sep 2004 A1
20040199249 Fell Oct 2004 A1
20040199250 Fell Oct 2004 A1
20040204766 Siebel Oct 2004 A1
20040230315 Ek Nov 2004 A1
20040243237 Unwin et al. Dec 2004 A1
20040267363 Fell et al. Dec 2004 A1
20050033424 Fell Feb 2005 A1
20050043816 Datta et al. Feb 2005 A1
20050048193 Li et al. Mar 2005 A1
20050049715 Ito Mar 2005 A1
20050070989 Lye et al. Mar 2005 A1
20050079200 Rathenow et al. Apr 2005 A1
20050085918 Soffiati et al. Apr 2005 A1
20050085922 Shappley et al. Apr 2005 A1
20050100578 Schmid et al. May 2005 A1
20050103765 Kawasaki May 2005 A1
20050112397 Rolfe May 2005 A1
20050123672 Justin et al. Jun 2005 A1
20050154471 Aram et al. Jul 2005 A1
20050169893 Koblish et al. Aug 2005 A1
20050170159 Ramsey et al. Aug 2005 A1
20050171604 Michalow Aug 2005 A1
20050177169 Fisher et al. Aug 2005 A1
20050192672 Wyss et al. Sep 2005 A1
20050203630 Pope et al. Sep 2005 A1
20060015187 Hunter et al. Jan 2006 A1
20060036251 Reiley Feb 2006 A1
20060036331 Lu et al. Feb 2006 A1
20060045903 Kadiyala et al. Mar 2006 A1
20060106419 Gingras May 2006 A1
20060116774 Jones et al. Jun 2006 A1
20060147332 Jones Jul 2006 A1
20060241776 Brown et al. Oct 2006 A1
20060241781 Brown et al. Oct 2006 A1
20060254200 Clarke et al. Nov 2006 A1
20070071733 Kandel et al. Mar 2007 A1
20070142914 Jones Jun 2007 A1
20070150068 Dong et al. Jun 2007 A1
20070156249 Lawrynowicz et al. Jul 2007 A1
20070173948 Meridew et al. Jul 2007 A1
20070203584 Bandyopadhyay et al. Aug 2007 A1
20070225390 Wang et al. Sep 2007 A1
20080004709 O'Neill et al. Jan 2008 A1
20080050412 Jones et al. Feb 2008 A1
20080071381 Buscher et al. Mar 2008 A1
20080161927 Savage et al. Jul 2008 A1
20080206862 Asgari Aug 2008 A1
20080288083 Axelsson et al. Nov 2008 A1
20090068245 Noble et al. Mar 2009 A1
20090087605 Ramsey et al. Apr 2009 A1
20090112315 Fang et al. Apr 2009 A1
20100057211 Cuckler et al. Mar 2010 A1
20100137990 Apatsidis Jun 2010 A1
20100161061 Hunt Jun 2010 A1
20100174377 Heuer Jul 2010 A1
20100256758 Gordon Oct 2010 A1
20100268337 Gordon Oct 2010 A1
20110076316 Sivananthan et al. Mar 2011 A1
20110200478 Billiet Aug 2011 A1
20110245930 Alley et al. Oct 2011 A1
20120022662 Conway et al. Jan 2012 A1
20120148987 Dolabdjian et al. Jun 2012 A1
20120215310 Sharp Aug 2012 A1
20120245697 Hunter et al. Sep 2012 A1
20120253474 Klein Oct 2012 A1
20130056912 O'Neill Mar 2013 A1
20130268085 Dong et al. Oct 2013 A1
20140228969 Engstrand Aug 2014 A1
20140262006 Biris Sep 2014 A1
20150258735 O'Neill Sep 2015 A1
20150374882 McDemus et al. Dec 2015 A1
20170095337 Pasini et al. Apr 2017 A1
20180055643 Castro Mar 2018 A1
20180228613 Jones Aug 2018 A1
20180280140 Jones et al. Oct 2018 A1
20180280145 Jones Oct 2018 A1
20180361510 Stamp et al. Dec 2018 A1
20190133770 Dion et al. May 2019 A1
20190290441 Tong Sep 2019 A1
20200086625 O'Neill Mar 2020 A1
20200179570 Heschel Jun 2020 A1
20200281724 Weber Sep 2020 A1
20200315662 Adam Oct 2020 A1
20200330235 Bauer Oct 2020 A1
20210106426 Zhang Apr 2021 A1
20210162731 O'Neill Jun 2021 A1
20210282930 Shi Sep 2021 A1
20220117753 Rucker Apr 2022 A1
20220142783 Ahmadi May 2022 A1
Foreign Referenced Citations (30)
Number Date Country
2295896 Jul 2000 CA
19502733 Mar 1996 DE
0 178 650 Apr 1986 EP
0295038 Dec 1988 EP
0 528 800 Mar 1993 EP
0761242 Mar 1997 EP
1247537 Oct 2002 EP
1 300 511 Apr 2003 EP
1418013 May 2004 EP
1426013 Jun 2004 EP
1455666 Sep 2004 EP
1493455 Jan 2005 EP
1683593 Jul 2006 EP
1806154 Jul 2007 EP
1949989 Jul 2008 EP
2255329 Oct 1990 JP
4041794 Feb 1992 JP
11287020 Oct 1999 JP
11348045 Dec 1999 JP
2001303751 Oct 2001 JP
2003293012 Oct 2003 JP
2006158953 Jun 2006 JP
2218242 Dec 2003 RU
9606881 Mar 1996 WO
9933641 Jul 1999 WO
02085246 Oct 2002 WO
2005084216 Sep 2005 WO
2005080029 Sep 2005 WO
2005087982 Sep 2005 WO
2007058160 May 2007 WO
Non-Patent Literature Citations (43)
Entry
Third Party Observation for EP05028133.6 dated Mar. 25, 2019, 3 pages.
Third Party Observation for EP05028133.6 dated May 18, 2020, 3 pages.
Williams, et al., “Advances in Modeling the Effects of Selected Parameters on the SLS Process,” Rapid Prototyping Journal, Jun. 1, 1998, pp. 90-100, vol. 4, No. 2.
Hollander et al., Structural mechanical and in vitro characterization of individually structured Ti-A1-4V produces by direct layer forming, Biomaterials, pp. 1-9, 2005.
Created and Designed by Shaman Gaspar, Maintained by Peter Fox, “Direct Laser Remelting” , “Project Web Site”, Using Lasers to Grow 3D object on Stainless Steel; The University of Liverpool 2002; http://mserc.liv.ac.uk/research/dlr/dlr_html.
Vureal et al., Plasma-sprayed oxide ceramics on steel substrates, Surface Coatings and Technology, 97 (1997) 347-354.
Patello-femoral Arthroplasty X-ray Results, Stryker Howmedica Osteonics, published on or before Apr. 5, 2011.
The Metals Handbook, Desk Edition, 2nd Edition, ASM International, 1998, p. 29.
Hawley's Condensed Chemical Dictionary, 14th edition. John Wiley & Sons, 2002. Definition: sintering.
Dr. Kerron Harvey, producer, Research Intelligence, The University of Liverpool, Issue 13, Jun. 2002.
H.J. Niu and I.T.H. Chang, “Selective Laser Sintering of Gas and Water Atomized High Speed Steel Powders, ” Scripta Materialia vol. 41, No. 1, (1999), pp. 25-30.
Meiners et al., “Direct Generation of Metal Parts and Tools by Selective Laser Powder Remelting (SLPR)”, W. Meiners, C. Over, K. Wissenbach, R. Poprawe, pp. 655-661 Austin, Texas, Aug. 9-11, 1999.
European Search Report and Written Opinion, EP05028133, dated May 11, 2010.
European Search Report and Written Opinion, EP10162970, dated Jun. 17, 2010.
R. Morgan, C.J. Sutcliffe, W. O'Neill, “Experimental investigatoin of nanosecond pulsed Nd:YAG laser re-melted pre-placed powder beds,” Rapid Prototyping Journal, vol. 7, No. 3, 2001, pp. 159-172.
N.K. Vail, L.D. Swain, W.C. fox, T.B. Aufdlemorte, G. Lee, J.W. Barlow, “Materials for biomedical applications,” Materials and Design, 20, 1999, pp. 123-132.
R.H. Morgan, A.J. Papworth, C. Sutcliffe, P. Fox, W. O'Neill, “High density net shape components by direct laser re-melting of single phase powders,” Journal of Materials Science, 37, 2002, pp. 3093-3100.
European Search Report and Written Opinion, EP06127218, dated May 6, 2010.
PCT/US2008/008955 International Search Report and Written Opinion dated Dec. 2, 2008.
PCT/US2008/008955 International Preliminary Report on Patentability dated Feb. 4, 2010.
C.K. Chua et al. Development of a Tissue Engineering Scaffold Structure Library for Rapid Prototyping. Parts 1 and 2, International Journal of Advanced Manufacturing Technology, Feb. 2003, vol. 21, pp. 291-312.
Bobyn et al., “The optimum pore size for the fixation of porous-surfaced metal implants by the ingrowth of bone”, Clinical Orthopaedics and Related Research, 150; 263-270 (1980).
Notice of Opposition for EP Application No. 06125422.3 dated Jul. 4, 2011.
Protek Cementless Replacement of the Acetabulum by E. Morscher, published on or before Apr. 5, 2011.
Interlocutory Decision for Application No. EP 06125422.3 dated Nov. 14, 2012.
European Examination Report for Application No. EP10162970.7 dated Dec. 3, 2013.
“Solid Freeform Fabrication”, IEEE Spectrum, Feb. 1999, pp. 34-43.
Custom Design and Manufacturing of Canine Knee Implants, <http://www.lib.ncsu.edu/resolver/1840.16/670>, Issued Dec. 2, 2003.
European Examination Report for Application No. EP10162970.7 dated Aug. 4, 2017.
Cheah et al., Automatic Algorithm for Generating Complex Polyhedral Scaffold Structures for Tissue Engineering, Tissue Engineering, vol. 10, No. 3/4, pp. 595-610, Mar. 2004.
Heinl et al., Cellular Ti-6Al-4V structures with interconnected macro porosity for bone implants fabricated by selective electron beam melting, Acta Biomaterialia, vol. 4, Issue 5, pp. 1536-1544, Sep. 2008.
Tuan et al., “Application of Micro CT and Computation Modeling in Bone Tissue Engineering”, Computer-Aided Design, vol. 37, No. 11, Sep. 2005, pp. 1151-1161.
Wang et al., “A Hybrid Geometric Modeling Method for Large Scale Conformal Cellular Structures,” ASME Design Engineering Technical Conferences, Sep. 2005, 7 pages.
Akamaru et al., “Healing of Autologous Bone in a Titanium Mesh Case Used in Anterior Column Reconstruction After Total Spondylectomy”, SPINE vol. 27, No. 13, 2002, pp. E329-E333.
McAfee et al., “Current Concepts Review: Interbody Fusion Cages in Reconstructive Operations on the Spine”, The Journal of Bone and Joint Surgery, vol. 81, Issue 6, Jun. 1999, pp. 859-880.
Lin et al., “Interbody Fusion Cage Design Using Integrated Global Layout and Local Microstructure Topology Optimization”, SPINE vol. 29, No. 16, pp. 1747-1754, Aug. 2004.
Williams et al., “CT evaluation of lumbar interbody fusion: Current concepts”, AJNR Am J Neuroradiol 26:2057-2066, Sep. 2005.
EBI Learning Center Cafe flyer, EBI Spine EBI & Interpore Cross, NASS Booth 801, prior to Sep. 27, 2005, Philadelphia, PA.
Stephen D. Kuslich, MD, “Lumbar Interbody Cage Fusion for Back Pain: An Update on the Bak (Bagby and Kuslich) System”, SPINE: State of the art reviews—vol. 13, No. 2, May 1999, pp. 295-311.
Zdeblick et al., “LT-CAGE—Lumbar Tapered Fusion Device—Surgical Technique”, Medtronic Sofamor Danek, 25 pages, Copyright 2000.
Cheung et al., “Spinal Instrumentation Overview in Lumbar Degenerative Disorders: Cages”, Chapter 26 / Spinal—Instrumentation Overview, Section IV/Surgery, Lumbar Spine: Official Publication of the International Society for the Study of the Lumbar Spine (3), 2004, pp. 286-291.
Kim et al., “Spinal Instrumentation Surgical Techniques”, Thieme Medical Publishers, Inc., New York, NY, Copyright 2005, 41 pages.
Lin et al., “Structural and mechanical evaluations of a topology optimized titanium interbody fusion cage fabricated by selective laser melting process”, Received Jan. 31, 2006, revised Aug. 25, 2006, accepted Dec. 2006, Published online Apr. 5, 2007 in Wiley Interscience (www.interscience.wiley.com). DOI: 10.1002/jbm.a.31231. 8 pages.
Related Publications (1)
Number Date Country
20200306048 A1 Oct 2020 US
Continuations (3)
Number Date Country
Parent 15788304 Oct 2017 US
Child 16900219 US
Parent 14276483 May 2014 US
Child 15788304 US
Parent 11295008 Dec 2005 US
Child 14276483 US