Patient-specific cutting block and method of manufacturing same

Information

  • Patent Grant
  • 10878965
  • Patent Number
    10,878,965
  • Date Filed
    Tuesday, January 15, 2019
    5 years ago
  • Date Issued
    Tuesday, December 29, 2020
    4 years ago
Abstract
A patient-specific cutting assembly comprises a model file including geometrical data of a bone of the patient, of an intramedullary canal of the bone, and a planned orientation of a cutting block. A fixing rod is adapted to be longitudinally inserted in and extending partially from the intramedullary canal. A patient-specific cutting block is connectable to the fixing rod. The patient-specific cutting block includes a structure having a patient specific geometry corresponding to the model file of the patient, the structure configured to be connected to a portion of the fixing rod projecting from the bone in a unique coupling orientation. A cutting guide is connected to the structure, the cutting guide being in the planned orientation when the structure is connected to the portion of the fixing rod projecting from the bone.
Description
TECHNICAL FIELD

The application relates generally to orthopedic surgery involving the preparation of bones with a view to fixing an implant thereon and, more particularly, to devices and tools developed in planning for assisting orthopedic surgery.


BACKGROUND

Before posing an implant onto a bone, such as during a knee or hip replacement surgery, the bone needs to be prepared. The preparation of the bone includes removing diseased bone, for example, and making additional cuts so that the bone has a shape matching that of an inside of the implant, or drilling holes, placing guides, etc for providing guidance landmarks to an operator. For instance, in knee implant surgery, transverse and frontal cut planes are made to match surfaces of an implant.


Determination of alterations to the bone, of the portions of the bone that need to be removed, of guides to be placed may be done prior to surgery using images of the bone of the patient, in pre-operative planning. The pre-operative planning may help in ensuring the precision and accuracy of the surgery, as bone alterations will influence the fit of the implant onto the bone. For example, a bone that has been improperly cut may lead to improper implant placement, resulting in conditions such as leg length discrepancy, improper gait, premature implant wear, and pain, to name a few.


SUMMARY

Therefore, in accordance with a first embodiment of the present disclosure, there is provided a method of creating a model of a patient-specific structure of a cutting block, the cutting block used for assisting an operator in cutting at least one plane in a bone of a patient, the method comprising: obtaining geometrical data of a bone and of an intramedullary canal of the bone; determining a penetration of a fixing rod to be inserted in and extending partially out from an intramedullary canal of the bone, the penetration based on the geometrical data of the intramedullary canal of the bone and on a geometry of the fixing rod; determining an orientation of a portion of the fixing rod projecting out of the bone relative to the bone based on the geometrical data of the bone, on the geometry of the fixing rod and on the penetration; and creating the model of the patient-specific structure of the cutting block using the geometrical data of the bone, a desired position and orientation of the at least one cut plane on the bone, and the orientation of the portion of the fixing rod projecting out of the bone.


Further in accordance with the first embodiment, creating the model comprises determining an orientation of a bore to be formed through the patient-specific structure, the bore being adapted to connect to the portion of the fixing rod in a unique coupling orientation.


Still further in accordance with the first embodiment, determining the orientation of the portion of the fixing rod projecting out of the bone relative to the bone comprises determining an orientation of the portion relative to a bone axis as the geometrical data of the bone.


Still further in accordance with the first embodiment, obtaining geometrical data of a bone comprises obtaining a mechanical axis of the bone.


Still further in accordance with the first embodiment, determining the orientation of the portion relative to the bone axis comprises obtaining a spatial angle between an axis of the portion of the fixing rod and the bone axis.


Still further in accordance with the first embodiment, instructions are created based on the model of the patient-specific structure for manufacturing the patient-specific structure.


Still further in accordance with the first embodiment, the patient-specific structure is manufactured based on the instructions.


Still further in accordance with the first embodiment, the desired position and orientation of the cutting plane of the bone is determined using a model of an implant.


Still further in accordance with the first embodiment, creating the model comprises modelling patient-specifically an attachment of the cutting guide to the patient-specific structure based on an orientation of the patient-specific structure relative to the bone and of geometrical data of the bone.


Still further in accordance with the first embodiment, instructions are created based on the patient-specific attachment model for manufacturing the patient-specific cutting attachment.


Still further in accordance with the first embodiment, the patient-specific cutting attachment is manufactured based on the instructions.


In accordance with a second embodiment of the present disclosure, there is provided a patient-specific cutting assembly, the assembly comprising: a model file including geometrical data of a bone of the patient, of an intramedullary canal of the bone, and a planned orientation of a cutting block; a fixing rod adapted to be longitudinally inserted in and extending partially from the intramedullary canal; and a patient-specific cutting block connectable to the fixing rod, the patient-specific cutting block including at least: a structure having a patient specific geometry corresponding to the model file of the patient, the structure configured to be connected to a portion of the fixing rod projecting from the bone in a unique coupling orientation; and a cutting guide connected to the structure, the cutting guide being in the planned orientation when the structure is connected to the portion of the fixing rod projecting from the bone.


Further in accordance with the second embodiment, the structure has a bore extending through opposed first and second faces thereof, the bore having a diameter allowing the fixing rod to be inserted thereinto, the bore being formed in the structure at an orientation based on the model file.


Still further in accordance with the second embodiment, an orientation of the bore in the structure is based on a predetermined bone axis.


Still further in accordance with the second embodiment, the predetermined bone axis is a mechanical axis of the bone.


Still further in accordance with the second embodiment, a face of the structure is adapted to abut the bone, the face of the structure has a shaped that is a negative of a surface of the bone obtained as the geometrical data of the bone of the patient.


Still further in accordance with the second embodiment, the fixing rod has a geometry that is a negative of an inner surface of the intramedullary canal obtained as the geometrical data of the intramedullary canal.


In accordance with a third embodiment of the present disclosure, there is provided a method of cutting a bone of a patient in preparation of placement of an implant onto the bone, the method comprising: inserting a fixing rod longitudinally in an intramedullary canal of the bone with a portion of the fixing rod extending outside the bone; connecting a patient-specific structure of a cutting block onto the portion of the fixing rod extending outside the bone and placing a cutting guide of the patient-specific cutting block in abutment with the bone in a unique coupling orientation; and cutting the bone with the cutting guide.


Further in accordance with the third embodiment, connecting the patient-specific structure comprises anchoring the patient-specific structure to the bone and removing the fixing rod.


In another aspect, there is provided a method of manufacturing a patient-specific structure of a cutting block, the structure providing a support to a cutting guide for cutting a plane in a bone of a patient, the method comprising: predicting an orientation of a fixing rod to be inserted in and extending partially from an intramedullary canal of the bone, the prediction of the orientation of the fixing rod being based on a known orientation of the intramedullary canal of the bone; determining an orientation of the fixing rod relative to a bone axis, the bone axis being determined using data of the bone, the determination of the orientation of the fixing rod being achieved by modelling the fixing rod inserted in the intramedullary canal; and modelling the patient-specific structure of the cutting block for manufacture thereof, the modelling including modelling a bore to be formed through the patient-specific structure, the bore being adapted to connect to the fixing rod, the bore having an orientation relative to the patient-specific structure dependent on the orientation of the fixing rod relative to the bone axis.


In yet another aspect, there is provided a patient-specific cutting assembly, the assembly comprising: a fixing rod adapted to be longitudinally inserted in and extending partially from an intramedullary canal of a bone of a patient; and a patient-specific cutting block connectable to the fixing rod, the patient-specific cutting block including: a structure comprising: opposed first and second faces; and a bore extending through opposed first and second faces, the bore having a diameter allowing the fixing rod to be inserted thereinto, the bore being formed in the structure at an orientation based on an orientation of the fixing rod should have when inserted in the intramedullary canal and on an orientation of a predetermined bone axis, the predetermined bone axis being determined using data of the bone, the structure when inserted into the fixing rod having a fixed orientation; and a cutting guide connected to the structure, the cutting guide being parallel to the opposed first and second faces, the cutting guide being at a distance from the structure based on an implant selected for the bone of the patient.


In yet another aspect, there is provided a method of cutting a bone of a patient in preparation of placement of an implant onto the bone, the method comprising: inserting a fixing rod longitudinally in an intramedullary canal of the bone with a portion of the fixing rod extending outside the bone; inserting a patient-specific structure of a cutting block onto the portion of the fixing rod extending outside the bone and placing a cutting guide of the patient-specific cutting block in abutment with the bone, the structure having opposed first and second faces and a bore therethrough, an orientation of the bore relative to the structure being predetermined as a function of an orientation of the fixing rod relative to the intramedullary canal and of a bone axis, the bone axis being predetermined using data of the bone, the bore providing a fixed patient-specific orientation of the structure relative to the bone, the cutting guide extending from the first face at a predetermined distance, the predetermined distance being dependent on the implant selected for the bone; and cutting the bone with the cutting guide.





DESCRIPTION OF THE DRAWINGS

Reference is now made to the accompanying figures in which:



FIG. 1 is a schematic view of a human femur;



FIG. 2 is an X-ray image of a femur;



FIG. 3 is a schematic view of a patient-specific cutting block for the femur of FIG. 1;



FIG. 4 is a schematic view of a fixing rod of the patient-specific cutting block of FIG. 3 inserted in the intramedullary canal of the femur of FIG. 1;



FIG. 5 is a schematic view of the femur of FIG. 1 shown with the patient-specific cutting block of FIG. 3 assembled to the fixing rod;



FIG. 6 is a schematic view of FIG. 5 shown from a different angle;



FIG. 7 is a flow chart of a method of manufacturing the patient-specific cutting block of FIG. 3; and



FIG. 8 is a flow chart of a method of cutting the femur of FIG. 1 with the patient-specific cutting block of FIG. 3.





DETAILED DESCRIPTION

The present disclosure will be made with reference to a human femur and a knee joint replacement surgery. It should be however understood that the disclosed devices and methods could be applied to human or animal bones other than the femur, to bone models, and implant surgeries other than knee joint replacement surgeries. Example of such bones include tibia, humerus and ulna, among others. The femur discussed herein being a 3-D component, spatial references will be made to “orientations”. By orientation, it should be understood spatial orientation defined by the three Euler angles (θ, φ, ψ) relative to a fixed frame of the bone. Also, references within this specification will be made to frontal plane (a.k.a. coronal plane), transverse plane (a.k.a. horizontal/vertical plane), and sagittal plane as commonly used as medical terminology.


With reference to FIG. 1, a human femur 10 is schematically shown along a frontal plane F. The femur 10 is the thigh bone and the longest bone in the body. A lower end 12 joins the tibia (not shown) to form the knee joint, while an upper end 14 is rounded into a femoral head 16 that fits into the acetabulum of the pelvis 19 (shown in FIG. 2) to form the hip joint. Just below the femoral head 16 is the femoral neck 18. The lower end 12 includes a lateral condyle 20 and a medial condyle 22, with a midpoint midway between the lateral condyle 20 and the medial condyle 22.


The femur 10, as other bones in the human body, is made of hard material, known as cortical bone, compact bone, forming the cortex of the bone. An inside of the bone contains a softer material called bone marrow. The bone marrow is contained in a portion called intramedullary canal 24 (shown in phantom in FIG. 1). The intramedullary canal 24 is non visible from the outside of the bone but can be seen on various medical imaging techniques such as X-rays used for example with magnetic resonance imagery to perform a 3-D reconstruction of the bone. The bone marrow being made of a material different from that of a rest of the bone, it may be contrasted out on the images. FIG. 2 shows an example of such imaging which enable to detect and define the intramedullary canal 24 in the bone, the bone portions being in a lighter shade of gray than the bone marrow. Hence, the geometry of the intramedullary canal 24 may be evaluated from the images, such as the X-rays.


The femur 10 is to be prepared in view of a knee joint replacement surgery by altering its knee-joint extremity in order to receive an implant (not shown) thereon. The lower end 12 is to be partially resurfaced to match a geometry of the implant for the implant to abut against the resurfaced knee joint in a predetermined position. The device and methods described herein allow tools such as a cutting block (a.k.a., positioning block, cut block, universal positioning block or tool) to be fabricated in part or as a whole as patient specific. The cutting block and other instruments described herein are said to be patient-specific, in that their geometries are modeled based on a planning for every patient's unique anatomy, using imaging techniques. Stated differently, the instruments such as the cutting block described hereinafter are developed subsequent to pre-operative steps by which a patient's anatomy is modeled and the implant position is defined. Hence, the instruments such as the cutting block described hereinafter have an identity related to a patient, and are most likely inadequate for being used with other patients, whereby the instruments are typically a one-time use instrument. Accordingly, the patient-specific instruments each have a model file of non-transient format which features a two-dimensional or three-dimensional model of the patient's anatomy resulting from pre-operative imaging. The specific geometry of the components of the patient-specific instruments are directly related to the contents of the model file. This means practically that data of the actual bone to be altered is used to manufacture portions or an entirety of the cutting block which once positioned relative to the femur 10, will be at a fixed predetermined and planned orientation and will guide a patient-specific cut of the femur 10.


Turning now to FIGS. 3 to 6, a patient-specific cutting assembly 30 includes a model file 31, a fixing rod 32 insertable in the intramedullary canal 24 of the femur 10, and a patient-specific cutting block 34 for cutting off portions of the bone, in preparation for implanting. The fixing rod 32 connects the patient-specific cutting block 34 to the femur 10.


The fixing rod 32 is a rigid rod selected to be inserted inside the intramedullary canal 24 of the femur 10. To that end, the fixing rod 32 is made of a biocompatible material. Examples of biocompatible materials include medical grade aluminum and medical grade titanium alloys. In order to be inserted inside the intramedullary canal 24, the fixing rod 32 is chosen to have a diameter smaller than that of the intramedullary canal 24 and to have a length allowing a portion to extend outside the femur 10. The diameter of the fixing rod 32 may not be chosen too small that the fixing rod 32 may radially displace in the intramedullary canal 24. At the same time, the diameter of the fixing rod 32 may not be chosen to large that the fixing rod 32 may alter the femur 10. Similarly, the length of the fixing rod 32 may not be chosen too short that the fixing rod 32 may not be secured in the intramedullary canal 24 and the cutting block 34 moves. The fixing rod 32, once inserted, should have a portion 32a extending from the femur 10 in order to attach a structure 36 of the cutting block 34 thereonto. The fixing rod 32 may be selected from a pool of already available rods or may be custom made to have a patient-specific geometry corresponding to that of the intramedullary canal 24. Hence, the fixing rod 32 may be one of the patient-specific instruments resulting from the pre-operative planning. In order to select the fixing rod 32, data on the femur 10 is analysed to determine a shape and size of the intramedullary canal 24. In one example, X-rays, such as the one of FIG. 2, are used to delimitate walls of the intramedullary canal 24, from which can be deduced a diameter and a length of the intramedullary canal 24. For instance, frontal and transverse X-rays may suffice in evaluating the geometry of the intramedullary canal 24 and predict a fit of the fixing rod 32 therein. In another example, a 3-D model of the intramedullary canal is created, and may be part of the model file 31, this embodiment being particularly useful when the fixing rod 32 has a geometry specific to the patient and thus shaped for custom and unique penetration in the intramedullary canal 24.


The patient-specific cutting block 34 includes the structure 36 to which one or more cutting guides 37 may be connected. Each of the cutting guide 37 has a cut slot, in which a blade may be inserted to guide in cutting the femur 10 along a plane of the cut slot. Other accessories may also be connected to the structure 36, such as drill guides, mill guides, reamer guides, in similar fashion to the cutting guide 37. The cutting guide 37 is removably connected to the structure 36 by an attachment 35. The cutting guide 37 and/or the attachment 35 may be selected from a pool of already made components or be patient-specific (i.e. manufactured based on patient's data), as a monolithic component with or without the structure 36. The attachment 35 may be connected to different locations on the structure 36 so as to orient cutting guide 37 and other alteration accessories to cut through different planes, such as the planes described above, or alter the bone at selected locations. In yet another embodiment, the cutting guide 37 are cut slots defined directly in the structure 36. According to another embodiment, temporary anchor holes are provided in the structure 36 to secure same to the femur F, after it has been positioned and oriented as planned relative to the femur F. This may allow the removal of the fixing rod 32, as the rod 32 could otherwise be in the way of cut blades. For example, lateral walls may project from the structure 36 for securing the structure 36 to medial/lateral portions of the femur F, which medial/lateral portions are not resurfaced during knee joint surgery.


In one non-limiting embodiment, the structure 36 has opposed first and second faces 38, 39. The second face 39 may abut the bone when installed onto the fixing rod 32. In order to provide a unique coupling orientation, the second face 39 may have a patient specific surface, being a negative of the bone it will abut, for unique complementary contact. Alternatively, the structure 36 may have abutments positioned as a function of the planning, again to ensure the unique coupling orientation. The structure 36 may made of a biocompatible material which may be same or different than the one used for the fixing rod 32. The structure 36 may have dimensions similar to that of the lower end 12 of the femur 10 against which it will abut (shown in FIG. 5). The structure 36 may be selected from a pool of already available structures or may be custom made based on preoperative data, such as model file 31, representative of the femur 10 it will be put onto.


The structure 36 includes a bore 40 (shown in FIG. 3) which is designed to position the structure 36 in a predetermined orientation to, in turn, position the cutting guide 37 along a desired cutting plane. The positioning of the bore 40 in the structure 36 may therefore be patient specific, such that the assembly of the structure 36 onto the fixing rod 32 via the bore 40 results in a planned unique coupling orientation of the structure 36 relative to the bone. When the patient-specific cutting assembly 30 is assembled onto the femur 10, the bore 40 receives the fixing rod 32. As such, the bore 40 is dimensioned to have a diameter larger than that of the fixing rod 32, for sliding movement thereon. In one embodiment, the diameter of the bore 40 is slightly larger than that of the fixing rod 32 to reduce any play therebetween. In addition, to provide the desired orientation of the structure 36, the bore 40 is disposed at a predetermined orientation relative to the opposed faces 38, 39 as mentioned above. It is also contemplated to provide a unique coupling orientation joint between the portion 32a of the fixing rod 32 and the bore 40, to reach the unique coupling orientation of the structure 36 relative to the bone. In the embodiment shown in the figures, the predetermined orientation corresponds to an angle α between the bore 40 and the opposed faces 38, 39. The angle α shown in the figures is an absolute angle. It may be decomposable into two angles projected respectively on the frontal plane F and a sagittal plane S (shown in FIG. 1). The angle α is chosen based on an orientation of the fixing rod 32 relative to the femur 10 when the fixing rod 32 is inserted in the intramedullary canal 24, i.e. axis A1, and on an orientation of a predetermined bone axis A2, for instance combining the angles along the transverse plane T and the frontal plane F. The axes A1 and A2 are shown in FIG. 4.


The axis A1 may be defined as the axis of the fixing rod 32 when the fixing rod 32 is inserted in the intramedullary canal 24. The orientation of the axis A1 may thus be determined preoperatively, after modelling the insertion of the fixing rod 32 into the intramedullary canal 24 using data of the femur 10 from, for example, pre-operative radiographic images, to determine an orientation of the intramedullary canal 24 and data of the selected fixing rod 32. In another example, the axis A1 may be defined as an axis passing at equidistance between walls of the intramedullary canal 24.


The axis A2 may be defined as an axis based on loads experienced by the femur 10 during normal use and/or connections to the other bones (pelvis and knee). For example, the axis A2 may be defined as the mechanical axis passing through the center of the femoral head 16 and the midpoint 21 (shown in FIG. 4) between the condyles 20, 22. Other definitions of the axis A2 are contemplated, as desired by the user of the system. The determination of the axis A2 may be using data of the bone, such as the X-rays or a 3-D model of the bone. Virtual modelling of the bone 10 and the loads may also be used to determine the axes A1 and A2.


The axes A1 and A2 are determined in a non-invasive pre-operative manner and before manufacturing the structure 36 so that the bore 40 may be formed in the structure 36 at the angle α desired such that once the fixing rod 32 and structure 36 are in place on the femur 10, the structure 36 provides the desired orientation for the cutting guide 37, simply by positioning the structure 36 on the fixing rod 32, without the subsequent need for intraoperative navigation to adjust the orientation of the structure 36.


In a femoral knee embodiment, the structure 36 may accommodate the attachment 35 in three distinct positions, so that the cutting guide 37 may be positioned to cut the femur 10 along the three different planes: transverse, frontal anterior and frontal posterior. The structure 36 could accommodate more or less than three distinct cutting positions, for examples by providing drill positions, and defines planes other than transverse and frontal. The planes corresponds to planes defined in the implant and through which the implant and the femur 10 will connect in coplanar fashion, and may include oblique planes. In the embodiment shown in the figures, the cutting guide 37 is disposed so as to perform cuts parallel to a transverse plane T. As shown in FIG. 5, the transverse plane T is parallel to the faces 38, 39 of the structure 36. The cutting guide 37 is disposed at a distance d (shown in FIG. 3) from the face 39 which is determined based on the implant selected (i.e. depth of the inside of the implant). The cutting guide 37 could be disposed along another plane after the cut along the transverse plane T. The other plane may be a plane perpendicular to the transverse plane T or at an angle with the transverse plane T. As such, the cutting guide 37 can be used to sequentially cut along different predetermined planes.


Turning now to FIG. 7, a method 50 of manufacturing the patient-specific cutting block 30 will be described. The method 50 is performed before surgery in order to provide a patient-specific bone cutting assembly or a patient-specific portion thereof.


According to 51, bone data is obtained, using imaging of the bone. For example, a model of the bone may be created. The bone data may include size, diameter and/or geometry of the intramedullary canal 24, and a model of the bone surface to be resurfaced, as well as axes, such as a mechanical axis of the femur F in the case of knee joint surgery.


The method 50 has a step 52 of determining the orientation of the fixing rod 32 as inserted in the intramedullary canal 24. The geometry of the intramedullary canal 24 may be determined from the bone data obtained at 51. Based on the dimension and shape of the intramedullary canal 24, a fixing rod 32 may be selected as described above. Alternatively, a fixing rod 32 specific to the patient may be designed in accordance with the geometry of the intramedullary canal 24 of the patient, ensure a specific and unique-orientation fit of the fixing rod 32 in the intramedullary canal 24. Modelling can be used to virtually insert the selected fixing rod 32 into the intramedullary canal 24 in order to determine an orientation of the portion 32a of the fixing rod 32 relative to the surrounding bone, for instance by determining axis A1. Other techniques can be used to determine the orientation of the portion 32a relative to femur F.


From step 52, the method 50 goes to step 54 where the orientation of the cut planes are determined. For example, the orientation of the cut planes may be based on the bone axis A2 (mechanical axis) based on an operator's preference in planning surgery, for instance in a fashion described above. For example, it may be desired that the bone axis A2 be normal to a transverse cut plane. Likewise, the anterior frontal and posterior frontal planes may be parallel to the bone axis A2, and perpendicular to the transverse cut plane. The bone axis A2 may have been drawn onto radiographic images or been virtually modelled onto a 3-D model of the femur 10 in step 51. Other ways to determine the orientation of the cut planes and/or indicate the bone axis A2 are contemplated. Then, the orientation of the bone axis A2 and of the fixing rod 32 inside the intramedullary canal 24 may be used to determine an orientation between them, for example using the angle α described above.


From step 54, the method 50 goes to step 56, where the patient-specific cutting block 30 is modeled based on the orientations of the axis A1 and A2 and on the orientation of the cut planes. As such, the method 50 may take into consideration the size of the implant that will be used. A portion (such as the structure 36) of the cutting block 30 or the entirety of the cutting block 30 can be modeled to be patient-specific. In the example below, the structure 36 is modeled to be patient specific. The model includes the bore 40 formed in the structure 36 at an angle related to the angle α, which indicates the orientation between the axes A1 and A2 and is thus patient specific as it was determined based on preoperative planning specific to the client. In one embodiment, the angle α corresponds to the orientation between the axis A1 and the axis A2 in the transverse plane and the frontal plane. However, modelling at step 54 may include only knowing relative orientations of the parts so as to select the structure 36 and form the bore 40 in accordance to the axis A1 and A2, and not necessarily 3-D modelling of the structure 36.


The method 50 may be followed by the steps of creating instructions based on the model of the structure 36 for manufacturing the structure 36, and manufacturing the structure 36 based on the instructions. The method 50 may also include selecting from a pool of attachments 35 or manufacturing the attachments 35 based on patient's data such that the cutting guide 37 is at the distance d according to the implant selected, the distance d being determined by the dimensions of the implant. Similarly, the cutting guide 37 may be selected form a pool of cutting guides 37 or manufactured based on patient's data and on the distance d. The implant may be selected based on patient data, and the implant characteristics may be provided so that the distance d may be determined.


Once the structure 36 is manufactured, the assembly of the structure 36, attachment 35 and cutting guide 32, if required, is performed intraoperatively.


Turning now to FIG. 8, a method 60 of cutting the femur 10 with the patient-specific cutting block 30 in preparation of placement of the implant thereonto will be described.


At step 62, with the femur resected or machined to expose the intramedullary canal, the fixing rod 32 is inserted longitudinally in the intramedullary canal 24 of the femur 10 such that the portion 32a of the fixing rod 32 extends outside the bone in the predicted manner.


At step 64, once the fixing rod 32 is inserted, the structure 36 may be installed onto the portion 32a, for instance until abutment with the lower end 12 of the femur 10. The structure 36, once inserted onto the fixing rod 32, may be rotated around the fixing rod 32 until being blocked in a desired position. For this purpose, the structure 36 may have abutments positioned to ensure that the structure 36 has a unique coupling orientation of abutment against the bone when installed onto the portion 32a. In one embodiment, the structure 36 is rotated so as to abut the posterior condyles. Other ways to position the structure 36 relative to the bone 10 are contemplated, such as complementary mating or abutment. The bore 40 provides a fixed patient-specific orientation of the structure 36 relative to the bone 10. As such, when the structure 36 is inserted, there may be no adjustment of the orientation of the structure 36 relative to the femur 10, as the structure 36 may necessarily adopt the unique coupling orientation. It may be necessary to rotate the structure 36 about the portion 32a to ensure that a desired orientation is reached. For this purpose, the structure 36 may have a visual marker to be aligned with the midpoint 21 (FIG. 4), or may have a projecting abutment that will abut against the bone in the predicted orientation, as alternatives to the patient specific second face 39. For instance, the attachment 35 may be positioned onto the structure 36 and the cutting guide 37 placed in abutment with the bone, to serve as the means for aligning the structure 36 in a degree of freedom of orientation that is about the axis of the fixing rod 32, if the portion 32a is round in cross-section. Other examples to set the rotation include one or more visual markers aligned with bony landmarks (e.g. epicondylar axis), surfaces on the patient-specific cutting block 30 matching a shape of the bone 10, abutment against the bone or cartilage, and abutment against posterior condyles.


In step 66, the bone may be cut along the transverse plane T (or another plane, depending on the cutting guide 37 position, as discussed above). The attachment 35 positions the cutting guide 37 at the distance d predetermined in function of the implant. It may be required that the structure 36 be pinned down to the bone, and the fixing rod 32 be removed, prior to cutting the bone.


The above device and methods allow to adapt the cutting tools to each patient so as to provide more precise cutting and therefore better fit of the implant. The above methods may be performed with already existing images of the bones or with new images of the bone. The patient-specific cutting block may be manufactured using a pool of structures, rods and cutting attachments and customising the bore orientation and the distance between the cutting guide and the structure.


The above description is meant to be exemplary only, and one skilled in the art will recognize that changes may be made to the embodiments described without departing from the scope of the invention disclosed. Other modifications which fall within the scope of the present invention will be apparent to those skilled in the art, in light of a review of this disclosure, and such modifications are intended to fall within the appended claims.

Claims
  • 1. A patient-specific cutting assembly, the assembly comprising: a model file including geometrical data of a bone of the patient, of an intramedullary canal of the bone, and a planned orientation of a cutting block;a fixing rod adapted to be longitudinally inserted in and extending partially from the intramedullary canal; anda patient-specific cutting block connectable to the fixing rod, the patient-specific cutting block including at least: a structure having a patient specific geometry corresponding to the model file of the patient, the structure configured to be connected to a portion of the fixing rod projecting from the bone to reach a unique coupling orientation with the structure coupled to the bone when the structure is connected to a portion of the fixing rod; anda cutting guide connected to the structure, the cutting guide being in the planned orientation when the structure is connected to the portion of the fixing rod projecting from the bone.
  • 2. The patient-specific cutting assembly according to claim 1, wherein the structure has a bore extending through opposed first and second faces thereof, the bore having a diameter allowing the fixing rod to be inserted thereinto, the bore being formed in the structure at an orientation based on the model file.
  • 3. The cutting assembly as defined in claim 2, wherein an orientation of the bore in the structure is based on a predetermined bone axis.
  • 4. The cutting assembly as defined in claim 3, wherein the predetermined bone axis is a mechanical axis of the bone.
  • 5. The cutting assembly as defined in claim 1, wherein a face of the structure is adapted to abut the bone, the face of the structure has a shaped that is a negative of a surface of the bone obtained as the geometrical data of the bone of the patient.
  • 6. The cutting assembly as defined in claim 1, wherein the fixing rod has a geometry that is a negative of an inner surface of the intramedullary canal obtained as the geometrical data of the intramedullary canal.
  • 7. A method of cutting a bone of a patient in preparation of placement of an implant onto the bone, the method comprising, sequentially: inserting a fixing rod longitudinally in an intramedullary canal of the bone with a portion of the fixing rod extending outside the bone;connecting a patient-specific structure of a cutting block onto the portion of the fixing rod extending outside the bone and placing a cutting guide of the patient-specific cutting block in abutment with the bone, while the structure is coupled to the bone in a unique coupling orientation; andcutting the bone with the cutting guide.
  • 8. The method as defined in claim 7, wherein connecting the patient-specific structure comprises anchoring the patient-specific structure to the bone and removing the fixing rod.
CROSS-REFERENCE TO RELATED APPLICATION

The present application is a divisional application of Ser. No. 14/729,505 filed on Jun. 3, 2015, which claims priority on U.S. Provisional Patent Application No. 62/007,124, filed on Jun. 3, 2014, and incorporated herein by reference.

US Referenced Citations (309)
Number Name Date Kind
4841975 Woolson Jun 1989 A
5098383 Hemmy et al. Mar 1992 A
5179915 Cohen Jan 1993 A
5490854 Fisher et al. Feb 1996 A
5768134 Swaelens et al. Jun 1998 A
5871018 Delp et al. Feb 1999 A
5916219 Matsuno et al. Jun 1999 A
5928240 Johnson Jul 1999 A
7357057 Chiang Apr 2008 B2
7468075 Lang et al. Dec 2008 B2
7510557 Bonutti Mar 2009 B1
7534263 Burdulis May 2009 B2
7618451 Berez et al. Nov 2009 B2
7634119 Tsougarakis et al. Dec 2009 B2
7717956 Lang May 2010 B2
7796791 Tsougarakis et al. Sep 2010 B2
7799077 Lang et al. Sep 2010 B2
7806896 Bonutti Oct 2010 B1
7806897 Bonutti Oct 2010 B1
7967868 White et al. Jun 2011 B2
7981158 Fitz et al. Jul 2011 B2
8062302 Lang et al. Nov 2011 B2
8066708 Lang et al. Nov 2011 B2
8070752 Metzger et al. Dec 2011 B2
8077950 Tsougarakis et al. Dec 2011 B2
8083745 Lang et al. Dec 2011 B2
8092465 Metzger et al. Jan 2012 B2
8094900 Steines et al. Jan 2012 B2
8105330 Fitz et al. Jan 2012 B2
8122582 Burdulis, Jr. et al. Feb 2012 B2
8133234 Meridew et al. Mar 2012 B2
8160345 Pavlovskaia et al. Apr 2012 B2
8175683 Roose May 2012 B2
8221430 Park et al. Jul 2012 B2
8234097 Steines et al. Jul 2012 B2
8241293 Stone et al. Aug 2012 B2
8282646 Schoenefeld et al. Oct 2012 B2
8298237 Schoenefeld Oct 2012 B2
8337501 Fitz et al. Dec 2012 B2
8337507 Lang et al. Dec 2012 B2
8343218 Lang et al. Jan 2013 B2
8366771 Burdulis et al. Feb 2013 B2
8377129 Fitz et al. Feb 2013 B2
8439926 Bojarski et al. May 2013 B2
8460304 Fitz et al. Jun 2013 B2
8480754 Bojarski et al. Jul 2013 B2
8500740 Bojarski et al. Aug 2013 B2
8529568 Bouadi Sep 2013 B2
8529630 Bojarski Sep 2013 B2
8585708 Fitz et al. Sep 2013 B2
8545569 Fitz et al. Oct 2013 B2
8551099 Lang Oct 2013 B2
8551102 Fitz et al. Oct 2013 B2
8551103 Fitz et al. Oct 2013 B2
8551169 Fitz et al. Oct 2013 B2
8556906 Fitz et al. Oct 2013 B2
8556907 Fitz et al. Oct 2013 B2
8556971 Lang Oct 2013 B2
8556983 Bojarski et al. Oct 2013 B2
8561278 Fitz et al. Oct 2013 B2
8562611 Fitz et al. Oct 2013 B2
8562618 Fitz et al. Oct 2013 B2
8568479 Fitz et al. Oct 2013 B2
8568480 Fitz et al. Oct 2013 B2
8617172 Fitz et al. Dec 2013 B2
8617242 Philipp Dec 2013 B2
8623026 Wong et al. Jan 2014 B2
8634617 Tsougarakis et al. Jan 2014 B2
8638998 Steines et al. Jan 2014 B2
8641716 Fitz et al. Feb 2014 B2
8657827 Fitz et al. Feb 2014 B2
8682052 Fitz et al. Mar 2014 B2
20030055502 Lang et al. Mar 2003 A1
20030216669 Lang et al. Nov 2003 A1
20040133276 Lang et al. Jul 2004 A1
20040138754 Lang et al. Jul 2004 A1
20040147927 Tsougarakis et al. Jul 2004 A1
20040153079 Tsougarakis et al. Aug 2004 A1
20040204644 Tsougarakis et al. Oct 2004 A1
20040204760 Fitz Oct 2004 A1
20040236424 Berez et al. Nov 2004 A1
20050203524 Penenberg Sep 2005 A1
20050234461 Burdulis et al. Oct 2005 A1
20050267584 Burdulis et al. Dec 2005 A1
20060111722 Bouadi May 2006 A1
20070083266 Lang Apr 2007 A1
20070100462 Lang et al. May 2007 A1
20070156171 Lang et al. Jul 2007 A1
20070157783 Chiang Jul 2007 A1
20070198022 Lang et al. Aug 2007 A1
20070226986 Park et al. Oct 2007 A1
20070233141 Park et al. Oct 2007 A1
20070233269 Steines et al. Oct 2007 A1
20070250169 Lang Oct 2007 A1
20080114370 Schoenefeld May 2008 A1
20080147072 Park et al. Jun 2008 A1
20080161815 Schoenefeld et al. Jul 2008 A1
20080195216 Philipp Aug 2008 A1
20080243127 Lang et al. Oct 2008 A1
20080275452 Lang et al. Nov 2008 A1
20080281328 Lang et al. Nov 2008 A1
20080281329 Fitz et al. Nov 2008 A1
20080281426 Fitz et al. Nov 2008 A1
20080287954 Kunz et al. Nov 2008 A1
20090024131 Metzgu et al. Jan 2009 A1
20090087276 Rose Apr 2009 A1
20090088753 Aram et al. Apr 2009 A1
20090088754 Aker et al. Apr 2009 A1
20090088755 Aker et al. Apr 2009 A1
20090088758 Bennett Apr 2009 A1
20090088759 Aram et al. Apr 2009 A1
20090088760 Aram et al. Apr 2009 A1
20090088761 Roose et al. Apr 2009 A1
20090088763 Aram et al. Apr 2009 A1
20090093816 Roose et al. Apr 2009 A1
20090099567 Zajac Apr 2009 A1
20090110498 Park et al. Apr 2009 A1
20090131941 Park et al. May 2009 A1
20090131942 Aker et al. May 2009 A1
20090138020 Park et al. May 2009 A1
20090157083 Park et al. Jun 2009 A1
20090222014 Bojarski et al. Sep 2009 A1
20090222016 Park et al. Sep 2009 A1
20090222103 Fitz et al. Sep 2009 A1
20090226068 Fitz et al. Sep 2009 A1
20090228113 Lang et al. Sep 2009 A1
20090254093 White et al. Oct 2009 A1
20090270868 Park et al. Oct 2009 A1
20090276045 Lang Nov 2009 A1
20090306676 Lang et al. Dec 2009 A1
20090307893 Burdulis, Jr. et al. Dec 2009 A1
20090312805 Lang et al. Dec 2009 A1
20100023015 Park Jan 2010 A1
20100042105 Park et al. Feb 2010 A1
20100049195 Park et al. Feb 2010 A1
20100054572 Tsougarakis et al. Mar 2010 A1
20100082035 Keefer Apr 2010 A1
20100087829 Metzger et al. Apr 2010 A1
20100152741 Park et al. Jun 2010 A1
20100152782 Stone et al. Jun 2010 A1
20100160917 Fitz et al. Jun 2010 A1
20100168754 Fitz et al. Jul 2010 A1
20100174376 Lang et al. Jul 2010 A1
20100185202 Lester et al. Jul 2010 A1
20100191244 White et al. Jul 2010 A1
20100211077 Couture Aug 2010 A1
20100212138 Carroll et al. Aug 2010 A1
20100217270 Polinski et al. Aug 2010 A1
20100217338 Carroll et al. Aug 2010 A1
20100228257 Bonutti Sep 2010 A1
20100234849 Bouadi Sep 2010 A1
20100256479 Park et al. Oct 2010 A1
20100262150 Lian Oct 2010 A1
20100274534 Steines et al. Oct 2010 A1
20100281678 Burdulis, Jr. et al. Nov 2010 A1
20100286700 Snider et al. Nov 2010 A1
20100298894 Bojarski et al. Nov 2010 A1
20100303313 Lang et al. Dec 2010 A1
20100303317 Tsougarakis et al. Dec 2010 A1
20100303324 Lang et al. Dec 2010 A1
20100305573 Fitz et al. Dec 2010 A1
20100305574 Fitz et al. Dec 2010 A1
20100305708 Lang et al. Dec 2010 A1
20100305907 Fitz et al. Dec 2010 A1
20100329530 Lang et al. Dec 2010 A1
20110015636 Katrana et al. Jan 2011 A1
20110015637 De Smedt et al. Jan 2011 A1
20110015639 Metzger et al. Jan 2011 A1
20110029091 Bojarski et al. Feb 2011 A1
20110029093 Bojarski et al. Feb 2011 A1
20110029116 Jordan et al. Feb 2011 A1
20110040168 Arnaud et al. Feb 2011 A1
20110054478 Vanasse et al. Mar 2011 A1
20110060341 Angibaud et al. Mar 2011 A1
20110066193 Lang et al. Mar 2011 A1
20110066245 Lang et al. Mar 2011 A1
20110071533 Metzger et al. Mar 2011 A1
20110071581 Lang et al. Mar 2011 A1
20110071645 Bojarski et al. Mar 2011 A1
20110071802 Bojarski et al. Mar 2011 A1
20110087332 Bojarski et al. Apr 2011 A1
20110092977 Salehi et al. Apr 2011 A1
20110093108 Ashby et al. Apr 2011 A1
20110106093 Romano et al. May 2011 A1
20110130761 Plaskos et al. Jun 2011 A1
20110144760 Wong et al. Jun 2011 A1
20110160736 Meridew et al. Jun 2011 A1
20110160867 Meridew et al. Jun 2011 A1
20110166578 Stone et al. Jul 2011 A1
20110172672 Dubeau et al. Jul 2011 A1
20110184419 Meridew et al. Jul 2011 A1
20110196377 Hodorek et al. Aug 2011 A1
20110213368 Fitz et al. Sep 2011 A1
20110213373 Fitz et al. Sep 2011 A1
20110213374 Fitz et al. Sep 2011 A1
20110213376 Maxson et al. Sep 2011 A1
20110213377 Lang et al. Sep 2011 A1
20110213427 Fitz et al. Sep 2011 A1
20110213428 Fitz et al. Sep 2011 A1
20110213429 Lang et al. Sep 2011 A1
20110213430 Lang et al. Sep 2011 A1
20110213431 Fitz et al. Sep 2011 A1
20110214279 Park et al. Sep 2011 A1
20110218539 Fitz et al. Sep 2011 A1
20110218545 Catanzarite et al. Sep 2011 A1
20110218584 Fitz et al. Sep 2011 A1
20110224674 White et al. Sep 2011 A1
20110230888 Lang et al. Sep 2011 A1
20110238073 Lang et al. Sep 2011 A1
20110245835 Dodds et al. Oct 2011 A1
20110266265 Lang Nov 2011 A1
20110275957 Bhandari Nov 2011 A1
20110295329 Fitz et al. Dec 2011 A1
20110295378 Bojarski et al. Dec 2011 A1
20110313423 Lang et al. Dec 2011 A1
20110313424 Bono et al. Dec 2011 A1
20110319897 Lang et al. Dec 2011 A1
20110319900 Lang et al. Dec 2011 A1
20120010711 Antonyshyn et al. Jan 2012 A1
20120029520 Lang et al. Feb 2012 A1
20120041445 Roose et al. Feb 2012 A1
20120041446 Wong et al. Feb 2012 A1
20120065640 Metzger et al. Mar 2012 A1
20120066892 Lang et al. Mar 2012 A1
20120071881 Lang et al. Mar 2012 A1
20120071882 Lang et al. Mar 2012 A1
20120071883 Lang et al. Mar 2012 A1
20120072185 Lang et al. Mar 2012 A1
20120078254 Ashby et al. Mar 2012 A1
20120078258 Lo et al. Mar 2012 A1
20120078259 Meridew Mar 2012 A1
20120093377 Tsougarakis et al. Apr 2012 A1
20120101503 Lang et al. Apr 2012 A1
20120109138 Meridew et al. May 2012 A1
20120116203 Vancraen et al. May 2012 A1
20120116562 Agnihotri et al. May 2012 A1
20120123422 Agnihotri et al. May 2012 A1
20120123423 Fryman May 2012 A1
20120130382 Iannotti et al. May 2012 A1
20120130687 Otto et al. May 2012 A1
20120141034 Iannotti et al. Jun 2012 A1
20120143197 Lang et al. Jun 2012 A1
20120151730 Fitz et al. Jun 2012 A1
20120158001 Burdulis, Jr. et al. Jun 2012 A1
20120165820 De Smedt et al. Jun 2012 A1
20120172884 Zheng et al. Jul 2012 A1
20120191205 Bojarski et al. Jul 2012 A1
20120191420 Bojarski et al. Jul 2012 A1
20120192401 Pavlovskaia et al. Aug 2012 A1
20120197260 Fitz et al. Aug 2012 A1
20120197408 Lang et al. Aug 2012 A1
20120201440 Steines et al. Aug 2012 A1
20120209276 Schuster Aug 2012 A1
20120209394 Bojarski et al. Aug 2012 A1
20120215226 Bonutti Aug 2012 A1
20120221008 Carroll et al. Aug 2012 A1
20120226283 Meridew et al. Sep 2012 A1
20120232669 Bojarski et al. Sep 2012 A1
20120232670 Bojarski et al. Sep 2012 A1
20120232671 Bojarski Sep 2012 A1
20120239045 Li Sep 2012 A1
20120245647 Kunz Sep 2012 A1
20120245699 Lang et al. Sep 2012 A1
20120259420 Lashure et al. Oct 2012 A1
20120265208 Smith Oct 2012 A1
20120271366 Katrana et al. Oct 2012 A1
20120276509 Iannotti et al. Nov 2012 A1
20120277751 Catanzarite et al. Nov 2012 A1
20120289966 Fitz et al. Nov 2012 A1
20120296337 Fitz et al. Nov 2012 A1
20120296339 Iannotti et al. Nov 2012 A1
20130018379 Fitz et al. Jan 2013 A1
20130018380 Fitz et al. Jan 2013 A1
20130018464 Fitz et al. Jan 2013 A1
20130023884 Fitz et al. Jan 2013 A1
20130024000 Bojarski et al. Jan 2013 A1
20130030419 Fitz et al. Jan 2013 A1
20130030441 Fitz et al. Jan 2013 A1
20130079781 Fitz et al. Mar 2013 A1
20130079876 Fitz et al. Mar 2013 A1
20130081247 Fitz et al. Apr 2013 A1
20130096562 Fitz et al. Apr 2013 A1
20130103363 Lang et al. Apr 2013 A1
20130110471 Lang et al. May 2013 A1
20130123792 Fitz et al. May 2013 A1
20130131681 Katrana May 2013 A1
20130184713 Bojarski et al. Jul 2013 A1
20130197870 Steines et al. Aug 2013 A1
20130211409 Burdulis, Jr. et al. Aug 2013 A1
20130211410 Landes et al. Aug 2013 A1
20130211531 Steines et al. Aug 2013 A1
20130245803 Lang Sep 2013 A1
20130253522 Bojarski et al. Sep 2013 A1
20130289570 Chao Oct 2013 A1
20130296874 Chao Nov 2013 A1
20130297031 Hafez Nov 2013 A1
20130317511 Bojarski et al. Nov 2013 A1
20130331850 Bojarski et al. Dec 2013 A1
20140005792 Lang et al. Jan 2014 A1
20140029814 Fitz et al. Jan 2014 A1
20140031826 Bojarski et al. Jan 2014 A1
20140039631 Bojarski et al. Feb 2014 A1
20140058396 Fitz et al. Feb 2014 A1
20140058397 Fitz et al. Feb 2014 A1
20140066935 Fitz et al. Mar 2014 A1
20140066936 Fitz et al. Mar 2014 A1
20140074441 Fitz et al. Mar 2014 A1
20140086780 Miller et al. Mar 2014 A1
20140257309 Aram Sep 2014 A1
Foreign Referenced Citations (222)
Number Date Country
2004293091 Jun 2005 AU
2004293104 Jun 2005 AU
2005309692 Jun 2006 AU
2005311558 Jun 2006 AU
2002310193 Mar 2007 AU
2006297137 Apr 2007 AU
2002310193 May 2007 AU
2007202573 Jun 2007 AU
2007212033 Aug 2007 AU
2007226924 Sep 2007 AU
2009221773 Sep 2009 AU
2009246474 Nov 2009 AU
2010201200 Apr 2010 AU
2011203237 Jul 2011 AU
2010217903 Sep 2011 AU
2010236263 Nov 2011 AU
2010264466 Feb 2012 AU
2010289706 Mar 2012 AU
2010315099 May 2012 AU
2010327987 Jun 2012 AU
2011203237 Oct 2012 AU
2012216829 Oct 2012 AU
2012217654 Oct 2013 AU
2007212033 Jan 2014 AU
2014200073 Jan 2014 AU
2012289973 Mar 2014 AU
2012296556 Mar 2014 AU
2501041 Apr 2004 CA
2505371 May 2004 CA
2505419 Jun 2004 CA
2506849 Jun 2004 CA
2546958 Jun 2005 CA
2546965 Jun 2005 CA
2804883 Jun 2005 CA
2588907 Jun 2006 CA
2590534 Jun 2006 CA
2623834 Apr 2007 CA
2641241 Aug 2007 CA
2646288 Sep 2007 CA
2717760 Sep 2009 CA
2765499 Dec 2010 CA
2771573 Mar 2011 CA
2779283 May 2011 CA
2782137 Jun 2011 CA
2546965 Mar 2013 CA
1728976 Feb 2006 CN
1729483 Feb 2006 CN
1729484 Feb 2006 CN
1913844 Feb 2007 CN
101111197 Jan 2008 CN
101384230 Mar 2009 CN
101442960 May 2009 CN
100502808 Jun 2009 CN
101878002 Nov 2010 CN
102006841 Apr 2011 CN
102125448 Jul 2011 CN
102405032 Apr 2012 CN
102448394 May 2012 CN
101420911 Jul 2012 CN
102599960 Jul 2012 CN
1913844 Sep 2012 CN
102711670 Oct 2012 CN
102724934 Oct 2012 CN
102805677 Dec 2012 CN
1729483 Oct 2013 CN
103476363 Dec 2013 CN
60336002 D1 Mar 2011 DE
60239674 D1 May 2011 DE
602004032166 D1 May 2011 DE
602005027391 D1 May 2011 DE
1555962 Jul 2005 EP
1558181 Aug 2005 EP
1567985 Aug 2005 EP
1575460 Sep 2005 EP
1686930 Aug 2006 EP
1686931 Aug 2006 EP
1389980 Apr 2007 EP
1814491 Aug 2007 EP
1833387 Sep 2007 EP
1686930 Oct 2007 EP
1686931 Jan 2008 EP
1928359 Jun 2008 EP
1951136 Aug 2008 EP
1981409 Oct 2008 EP
1996121 Dec 2008 EP
2114312 Nov 2009 EP
2124764 Dec 2009 EP
1928359 Oct 2010 EP
2259753 Dec 2010 EP
2265199 Dec 2010 EP
1555962 Feb 2011 EP
2292188 Mar 2011 EP
2292189 Mar 2011 EP
1389980 Apr 2011 EP
1686930 Apr 2011 EP
1833387 Apr 2011 EP
2303193 Apr 2011 EP
2316357 May 2011 EP
2324799 May 2011 EP
2335654 Jun 2011 EP
2403434 Jan 2012 EP
2405865 Jan 2012 EP
2419035 Feb 2012 EP
2265199 Mar 2012 EP
2303193 Mar 2012 EP
2259753 Apr 2012 EP
2292188 May 2012 EP
2292189 May 2012 EP
2445451 May 2012 EP
2470126 Jul 2012 EP
2496183 Sep 2012 EP
2509539 Oct 2012 EP
2512381 Oct 2012 EP
2324799 Jan 2013 EP
2419035 Jan 2013 EP
2445451 Mar 2013 EP
2403434 Apr 2013 EP
2591756 May 2013 EP
2496183 Dec 2013 EP
2512381 Dec 2013 EP
2649951 Dec 2013 EP
2649951 Dec 2013 EP
2671520 Dec 2013 EP
2671521 Dec 2013 EP
2671522 Dec 2013 EP
2114312 Jan 2014 EP
2710967 Mar 2014 EP
2484042 Mar 2012 GB
2489884 Oct 2012 GB
201213674 Oct 2012 GB
2484042 Mar 2014 GB
1059882 Aug 2011 HK
1072710 Aug 2011 HK
1087324 Nov 2011 HK
1104776 Nov 2011 HK
2006510403 Mar 2006 JP
2007514470 Jun 2007 JP
2011519713 Jul 2011 JP
2011224384 Nov 2011 JP
2012091033 May 2012 JP
2012176318 Sep 2012 JP
5053515 Oct 2012 JP
2012187415 Oct 2012 JP
2012523897 Oct 2012 JP
5074036 Nov 2012 JP
2012531265 Dec 2012 JP
2013503007 Jan 2013 JP
5148284 Feb 2013 JP
5198069 May 2013 JP
2014000425 Jan 2014 JP
20050072500 Jul 2005 KR
20050084024 Aug 2005 KR
20120090997 Aug 2012 KR
20120102576 Sep 2012 KR
2012007140 Jan 2013 MX
597261 Nov 2013 NZ
173840 Sep 2011 SG
175229 Nov 2011 SG
176833 Jan 2012 SG
178836 Apr 2012 SG
193484 Oct 2013 SG
200509870 Mar 2005 TW
1231755 May 2005 TW
200800123 Jan 2008 TW
1330075 Sep 2010 TW
2004049981 Jun 2004 WO
2004051301 Jun 2004 WO
2005051239 Jun 2005 WO
2005051240 Jun 2005 WO
2006058057 Jun 2006 WO
2006060795 Jun 2006 WO
2006058057 Jul 2006 WO
2007041375 Apr 2007 WO
2007062103 May 2007 WO
2007092841 Aug 2007 WO
2007109641 Sep 2007 WO
2007092841 Nov 2007 WO
2007109641 Dec 2007 WO
2008101090 Aug 2008 WO
2008112996 Sep 2008 WO
2008101090 Nov 2008 WO
2008157412 Dec 2008 WO
2007041375 Apr 2009 WO
2008157412 Apr 2009 WO
2009111626 Sep 2009 WO
2009111639 Sep 2009 WO
2009111656 Sep 2009 WO
2009140294 Nov 2009 WO
2009111626 Jan 2010 WO
2010099231 Sep 2010 WO
2010099353 Sep 2010 WO
2010121147 Oct 2010 WO
2010099231 Nov 2010 WO
2011028624 Mar 2011 WO
2011056995 May 2011 WO
2011072235 Jun 2011 WO
2011075697 Jun 2011 WO
2011056995 Sep 2011 WO
2011075697 Oct 2011 WO
2011072235 Dec 2011 WO
2012112694 Aug 2012 WO
2012112694 Aug 2012 WO
2012112698 Aug 2012 WO
2012112701 Aug 2012 WO
2012112702 Aug 2012 WO
2012112694 Jan 2013 WO
2012112701 Jan 2013 WO
2012112702 Jan 2013 WO
2013020026 Feb 2013 WO
2013025814 Feb 2013 WO
2012112698 Mar 2013 WO
2013056036 Apr 2013 WO
2013119790 Aug 2013 WO
2013119865 Aug 2013 WO
2013136302 Sep 2013 WO
2013131066 Sep 2013 WO
2013152341 Oct 2013 WO
2013155500 Oct 2013 WO
2013155501 Oct 2013 WO
2014008444 Jan 2014 WO
2014035991 Mar 2014 WO
2014047514 Mar 2014 WO
Non-Patent Literature Citations (1)
Entry
Hofmann et al, “Natural-Knee II System”, Intermedics Orthopedics, Austin, TX, 1995.
Related Publications (1)
Number Date Country
20190148022 A1 May 2019 US
Provisional Applications (1)
Number Date Country
62007124 Jun 2014 US
Divisions (1)
Number Date Country
Parent 14729505 Jun 2015 US
Child 16248051 US