Latent mobile bearing for prosthetic device

Information

  • Patent Grant
  • 9498341
  • Patent Number
    9,498,341
  • Date Filed
    Friday, March 20, 2015
    9 years ago
  • Date Issued
    Tuesday, November 22, 2016
    7 years ago
Abstract
A prosthetic device for an anatomical feature includes a prosthetic member able to be fixed to the anatomical feature. The device also includes a bearing including a bearing surface able to support an articulating surface for articulation thereon. Additionally, the device includes a bearing restraining member that limits movement of the bearing relative to the prosthetic member at a first time. The bearing restraining member also allows for increased movement of the bearing relative to the prosthetic member at a second time without surgical intervention.
Description
FIELD

The following relates to a prosthetic device and, more particularly, to a latent mobile bearing for a prosthetic device.


BACKGROUND

The statements in this section merely provide background information related to the present disclosure and may not constitute prior art.


Prosthetic joints can reduce pain due to arthritis, deterioration, deformation, and the like, and can improve mobility of the joint. Oftentimes, prosthetic joints can include certain implantable prosthetic members that are fixed to the patient's anatomy. For instance, knee joint prosthetic devices can include a femoral component fixed to the patient's femur and a tibial component fixed to the patient's tibia. Also, the device can include a bearing disposed between the femoral and tibial components. The bearing can be supported by the tibial component, and the bearing can include a bearing surface. An articulating surface of the femoral component can articulate on the bearing surface of the bearing.


In some cases, the bearing can be fixedly coupled to the tibial component. In other cases, the bearing can be moveably coupled to the tibial component. Both types of bearings can be of benefit to the patient for providing mobility of the joint. For some patients, the mobile bearing provides better and more natural movement of the articulating joint.


The following discloses a prosthetic device with a bearing that allows for improved articulation of the joint. The prosthetic device also promotes healing of the anatomical tissue.


SUMMARY

A prosthetic device for an anatomical feature is disclosed. The device includes a prosthetic member able to be fixed to the anatomical feature. The device also includes a bearing including a bearing surface able to support an articulating surface for articulation thereon. Additionally, the device includes a bearing restraining member that limits movement of the bearing relative to the prosthetic member at a first time. The bearing restraining member also allows for increased movement of the bearing relative to the prosthetic member at a second time without surgical intervention.


Also, a method of implanting a prosthetic device for an anatomical feature is disclosed. The method includes implanting a prosthetic member in the anatomical feature. Furthermore, the method includes supporting a bearing with the prosthetic member such that movement of the bearing relative to the prosthetic member is limited at a first time and such that allowable movement of the bearing relative to the prosthetic member is increased at a second time without surgical intervention. Moreover, the method includes supporting an articulating surface with the bearing.


Still further, a knee joint prosthetic device supporting movement between a femur and a tibia of a patient is disclosed. The knee joint prosthetic device includes a tibial prosthetic member that can be implanted on the tibia and a femoral prosthetic member that can be implanted on the femur. The femoral prosthetic member includes an articulating surface. Additionally, the prosthetic device includes a bearing supported by the tibial prosthetic member. The bearing includes a bearing surface able to support the articulating surface for articulation thereon. Moreover, the prosthetic device includes a bearing restraining member that limits linear and rotational movement of the bearing relative to the tibial prosthetic member at a first time. The bearing restraining member also allows for increased linear and rotational movement of the bearing relative to the prosthetic member at a second time without surgical intervention.


Further areas of applicability will become apparent from the description provided herein. It should be understood that the description and specific examples are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.





DRAWINGS

The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.



FIG. 1 is a perspective view of an exemplary embodiment of a prosthetic device;



FIG. 2 is a side view of the prosthetic device of FIG. 1;



FIG. 3 is a top view of the prosthetic device of FIG. 1;



FIG. 4A is a section view of a resorbing member of the prosthetic device of FIG. 1;



FIG. 4B is a section view of the prosthetic device of FIG. 4A after the resorbing member has resorbed;



FIG. 5A is a section view of another exemplary embodiment of a resorbing member of the prosthetic device of FIG. 1;



FIG. 5B is a section view of the prosthetic device of FIG. 5A after the resorbing member has resorbed;



FIG. 6A is a section view of another exemplary embodiment of a resorbing member of the prosthetic device of FIG. 1;



FIG. 6B is a section view of the prosthetic device of FIG. 6A after the resorbing member has resorbed;



FIG. 7 is a top view of another exemplary embodiment of a resorbing member of the prosthetic device of FIG. 1;



FIG. 8A is a section view of the resorbing member of the prosthetic device of FIG. 7;



FIG. 8B is a section view of the prosthetic device of FIG. 7A after the resorbing member has resorbed;



FIG. 9 is a top view of another exemplary embodiment of a resorbing member of the prosthetic device of FIG. 1;



FIG. 10 is a section view of another exemplary embodiment of a resorbing member of the prosthetic device of FIG. 1; and





DETAILED DESCRIPTION

The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses. It should be understood that throughout the drawings, corresponding reference numerals indicate like or corresponding parts and features.


Referring now to FIGS. 1 and 2, a prosthetic device 10 for an anatomical feature 12 (e.g., a leg) is illustrated according to various exemplary embodiments of the present disclosure. As shown, the prosthetic device 10 can be a prosthetic knee joint 14 (FIG. 2); however, it will be appreciated that the prosthetic device 10 can be of any suitable type for any suitable joint of a patient. Moreover, it will be appreciated that the knee joint 14 can be a cruciate retaining (CR) joint, a posterior stabilized (PS) joint, a fully constrained joint, a hinged knee joint, or any other suitable knee joint 14.


In the embodiments shown, the prosthetic device 10 can include a first prosthetic member 16. The first prosthetic member 16 can be made out of cobalt chromium, titanium or any other suitable biocompatible material. The first prosthetic member 16 can be a first femoral prosthetic member 16 and can be implanted and fixed to an inferior end of a resected femur 18 (FIG. 2). More specifically, the first prosthetic member 16 can include a bone engaging surface 19 that engages the femur 18, and the first prosthetic member 16 can be fixed to the femur 18 via fasteners, bone cement, or any other suitable means. The first prosthetic member 16 can also include one or more articulating surfaces 26 on a side opposite the bone engaging surface 19. For instance, the articulating surfaces 26 can be substantially similar to anatomical medial and lateral condylar surfaces.


Furthermore, the prosthetic device 10 can include a second prosthetic member 20. The second prosthetic member 20 can be made out of cobalt chromium, titanium or any other suitable biocompatible material. The second prosthetic member 20 can be a second tibial prosthetic member 20 and can be implanted and fixed to a superior end of a resected tibia 22 (FIG. 2). The second prosthetic member 20 can include a tray 23 and a post 25. The tray 23 can be relatively flat and can include a bone engaging surface 27 that engages the tibia 22. The tray 23 can also include a superior surface 29 opposite the bone engaging surface 27. The post 25 can be fixed to the tray and can be generally cylindrical. The post 25 can extend inferiorly from the tray 23 and can be received in a corresponding opening in the tibia 22 to fix the second prosthetic member 20 to the tibia 22. The second prosthetic member 20 can also be fixed to the tibia 22 by fasteners, bone cement, or any other suitable means. In addition, the second prosthetic member 20 can include a guide post 33 that is generally cylindrical. The guide post 33 can extend superiorly from the tray 23. It will be appreciated that the guide post 33 can be included, especially, for posterior-stabilized and fully constrained prosthetic knee joint 14; however, it will be appreciated that the guide post 33 may not be necessary for another prosthetic knee joint 14, which nevertheless falls within the scope of the present disclosure.


Moreover, the prosthetic device 10 can include a bearing 24. The bearing 24 can be made out of polyethylene (e.g., ultra high molecular weight polyethylene (UHMWPE)) or any other suitable material. The bearing 24 can include an inferior surface 31 that is supported on and that abuts the superior surface 29 of the tray 23. The bearing 24 can also include a bearing surface 28 opposite the inferior surface 31. The bearing surface 28 can be three-dimensionally and concavely curved. The bearing surface 28 can correspond in shape to the articulating surface 26 of the first prosthetic member 16. As such, the articulating surface 26 can be slidingly supported on the bearing surface 28, and the bearing surface 28 can support the articulating surface 26 for articulation thereon to replicate anatomical movement of the joint 14. Moreover, the bearing 24 can include a through hole 35 that extends between the bearing surface 28 and the inferior surface 31. The guide post 33 can be received within the through hole 35. As shown, the through hole 35 can be larger than the guide post 33 to allow the bearing 24 to move relative to the tray 23 as will be discussed in greater detail.


In addition, the prosthetic device 10 can include one or more bearing restraining mechanisms or members 37. As will be discussed, the bearing restraining members 37 can limit movement of the bearing 24 relative to the tray 23 at a first time (e.g., when the prosthetic device 10 is first implanted). Also, the bearing restraining member 37 can eventually (i.e., at a second time) allow for increased movement of the bearing 24 relative to the tray 23 without surgical intervention.


For instance, the restraining members 37 can initially fix the bearing 24 and tray 23 together such that the relative range of movement (i.e., range of motion, degree of freedom, etc.) is substantially zero millimeters. Then, weeks after surgery, the restraining members 37 can allow the relative range of movement (i.e., the relative range of motion, degree of freedom, etc.) to be greater than zero millimeters. Also, in some embodiments, the restraining members 37 can initially limit the relative range of movement to X millimeters, and the restraining members 37 can eventually allow for a relative range of movement of X+1 millimeters. Still further, in some embodiments, the restraining members 37 can initially allow for a first type of relative movement (e.g., anterior-posterior movement) while limiting a second type of relative movement (e.g., rotational), and the restraining members 37 can eventually allow for both types of relative movement.


In some embodiments, the bearing restraining members 37 can be resorbing members 30 shown schematically in FIG. 2. The resorbing members 30 can be made out of any suitable biologically compatible material that resorbs or partially resorbs in the body. The terms “resorbing,” “resorption,” “resorb,” and other related terms are defined herein as either partial or total loss of volume, strength, hardness, durometer, etc. over time.


The resorbing members 30 can be made out of any suitable resorbing material. This set of materials includes, without limitation, categories of suitable materials such as resorbable polymer materials, resorbable ceramic materials, resorbable metals, biological materials and combinations thereof. Also, the resorbing members 30 can be made out of synthetic materials such as resorbable monomers and polymers, non-limiting examples of which include: certain polyesters, including but not limited to polylactic acid and polyglycolic acid, polycaprolactone, certain polyurethanes, protein or amino acid based polymers, polysaccharides, hyaluronic acid, polyethylene glycol, activated or modified forms of these materials, combinations of these materials, co-polymers and ter-polymers of these materials, and these materials in combination with other materials. Moreover, in some embodiments, the resorbing members 30 can be made out of LACTOSORB®, which is commercially available from Biomet of Warsaw, Ind. and is a co-polymer of polylactic acid and polyglycolic acid. Non-limiting examples of resorbable ceramics include calcium containing ceramics such as certain calcium phosphates, calcium sodium phosphates, calcium sulfates, and combinations thereof. A non-limiting example of a potentially suitable resorbable metal includes magnesium alloys. Non-limiting examples of suitable biological materials may include cellulose, gelatin, autograft tissue, allograft tissue, xenogenic material, and extra cellular matrices (ECMs). Exemplary non-limiting examples of such ECMs include, without limitation, porcine small intestine submucosa (SIS), xenogeneic small intestine submucosa (xSIS), urinary bladder submucosa (UBS), laminated intestinal submucosa, glutaraldehyde-treated bovine pericardium (GLBP), and other acellular collagen containing materials. The resorbing members 30 can be layered, molded, formed, braided, perforated, multilaminated, grafted or otherwise manipulated to achieve the desired properties and dimensions.


The resorbing members 30 can be disposed between the bearing 24 and the second prosthetic member 20 and can at least temporarily couple the bearing 24 to the second prosthetic member 20 so that the bearing 24 can be fixed or immovable relative to the tray 23. As such, the resorbing members 30 can temporarily limit a range of movement of the bearing 24 relative to the second prosthetic member 20. Also, as will be discussed in greater detail below, the resorbing members 30 can resorb (i.e., reduce in size and be resorbed within the patient's body) to allow movement of the bearing 24 relative to the second prosthetic member 20 within an increased range of motion.


Accordingly, as will be discussed, the resorbing members 30 can be strong enough to limit movement of the bearing 24 relative to the second prosthetic member 20. For instance, when the prosthetic device 10 is initially implanted, the resorbing members 30 can substantially fix the bearing 24 to the second prosthetic member 20 to promote healing of soft tissue, etc. Over time, the resorbing members 30 can resorb, and the bearing 24 can move relative to the second prosthetic member 20. This movement of the bearing 24 can allow for improved mobility of the joint 14 as discussed in U.S. Pat. No. 6,972,039, filed Jul. 1, 2002, to Metzger et al., the disclosure of which is hereby incorporated by reference in its entirety.


As shown in FIGS. 3 and 4A, the resorbing member 30 can have a block-like, or any other suitable shape. Also, the superior surface 29 of the tray 23 can include an opening 32 (e.g., a recess), and the inferior surface 31 of the bearing 24 can include a similar opening 34 (e.g., a recess). The openings 32, 34 can align when the bearing 24 is supported on the tray 23, and the resorbing member 30 can be received in both openings 32, 34 (FIG. 4A). In some embodiments represented in FIG. 3, the resorbing members 30 can be disposed anteriorly and posteriorly from the guide post 33. However, it will be appreciated that the resorbing members 30 can be disposed at any suitable position in the prosthetic device 10.


Moreover, in some embodiments, the resorbing members 30 can be inserted between the bearing 24 and the second prosthetic member 20 during surgery, while the prosthetic device 10 is being implanted. In other embodiments, the resorbing member 30 can be made of a liquid material that can be injected with a needle (not shown) between the bearing 24 and the second prosthetic member 20, and the resorbing member 30 can subsequently harden and cure into a solid state to limit the bearing 24 against movement relative to the prosthetic member 20.


As shown in FIGS. 3 and 4A, the size and shape of the resorbing member 30 substantially matches the combined size and shape of the openings 32, 34. Thus, the resorbing member 30 can substantially fill the openings 32, 34, and the resorbing member 30 can substantially fix the bearing 24 against movement relative to the second prosthetic member 20. For instance, the resorbing member 30 can fix the bearing 24 against linear movement in the anterior-posterior direction as represented by the vertical, double-headed arrow in FIG. 3. Also, the resorbing member 30 can fix the bearing 24 against rotational movement about the guide post 33 as represented by the curved, double-headed arrow in FIG. 3.


Then, as shown in FIG. 4B, the resorbing member 30 can resorb, leaving the bearing 24 free to move relative to the second prosthetic member 20 in an increased range of movement. In some embodiments, once the resorbing member 30 resorbs, the bearing 24 can move in a linear, anterior-posterior range of movement as represented by the vertical, double-headed arrow in FIG. 3. Also, in some embodiments, once the resorbing member 30 resorbs, the bearing 24 can rotate about the guide post 33 as represented by the curved, double-headed arrow in FIG. 3. However, it will be appreciated that the prosthetic device 10 can be configured such that the bearing 24 moves in any direction and within any range of movement relative to the second prosthetic member 20 once the resorbing member 30 resorbs.


Furthermore, in some embodiments, the resorbing member 30 can automatically resorb over time. In other embodiments, the resorbing member 30 can selectively resorb at a predetermined time. In the latter case, a surgeon can inject a substance into the patient, which causes the resorbing member 30 to begin to resorb. More specifically, the resorbing member 30 can be made from or include a magnesium alloy, and the surgeon can inject a saline buffer that sets off resorption. Furthermore, the resorbing member 30 can be made from or include calcium phosphate or calcium carbonate, and a citric acid can be injected to resorb and dissolve the resorbing member 30 relatively quickly.


Referring now to FIGS. 5A and 5B, further exemplary embodiments of the prosthetic device 110 are illustrated. Components that are similar to those of the embodiments of FIGS. 1-4B are indicated with similar reference numbers, increased by 100.


As shown in FIG. 5A, the prosthetic device 110 can include a first resorbing member 130a and a second resorbing member 130b. The first resorbing member 130a can be fixed to the tray 123 and can project into the opening 132. Likewise, the second resorbing member 130b can be fixed to the bearing 124 and can project into the opening 134. When the bearing 124 is supported on the tray 123, the first and second resorbing members 130a, 130b can abut against each other.


The prosthetic device 110 can also include a biasing member 138. The biasing member 138 can couple the bearing 124 and the second prosthetic member 120 to limit relative movement as discussed above. Also, the biasing member 138 can be biased to allow increased relative movement between the bearing 124 and the second prosthetic member 120 once the resorbing members 130a, 130b resorb.


The biasing member 138 can be of any suitable type, such as a compression spring. As shown in the exemplary embodiments illustrated, the biasing member 138 can be a resilient C-shaped clip. The biasing member 138 can engage the first and second resorbing members 130a, 130b and compress the first and second resorbing members 130a, 130b toward each other. As such, the biasing member 138 can bias the bearing 124 toward the second prosthetic member 120 to limit movement of the bearing 124 relative to the second prosthetic member 120.


Then, as shown in FIG. 5B, the resorbing members 130a, 130b can resorb, allowing the biasing member 138 to move into one of the openings 132, 134. For instance, as shown in FIG. 5B, the biasing member 138 can move completely into the opening 132 and out of the opening 134. This can allow the bearing 124 to move relative to the second prosthetic member 120 as discussed above. In some embodiments, the biasing member 138 can be tethered or otherwise attached to either the bearing 124 or the second prosthetic member 120 so that the biasing member 138 is retained within either the opening 132 or the opening 134, respectively, after resorption. Also, in some embodiments, the biasing member 138 can be removed from the openings 132, 134 by a surgeon after resorption of the members 130a, 130b. Also, in some embodiments, the biasing member 138 itself can be made of resorbable material.


Referring now to FIGS. 6A and 6B, further exemplary embodiments of the prosthetic device 210 are illustrated. Components that are similar to those of the embodiments of FIGS. 5A and 5B are indicated with similar reference numbers, increased by 100.


As shown in FIG. 6A, the biasing member 238 can be a tab that is fixed to the tray 223. The biasing member 238 can resiliently bend in a superior direction toward the bearing 224 to be received within the opening 234. Also, the resorbing member 230 can be wedged between the biasing member 238 and the tray 223 to thereby push the biasing member 238 and hold the biasing member 238 within the opening 234. As such, the biasing member 238 can engage the bearing 224 to limit movement of the bearing 224 relative to the second prosthetic member 220.


Then, as shown in FIG. 6B, when the resorbing member 230 resorbs, the biasing member 238 can resiliently recover to move back into the opening 232 of the second prosthetic member 220. Thus, the bearing 224 can move relative to the second prosthetic member 220 as discussed above.


It will be appreciated that the biasing member 238 could be fixed to the bearing 224, and the resorbing member 230 could push the biasing member 238 into the opening 232 of the second prosthetic member 220 without departing from the scope of the present disclosure.


Furthermore, in the embodiments of FIGS. 6A and 6B, the biasing member 238 is smaller than the opening 234. As such, the bearing 224 can move relative to the second prosthetic member 220 over a first range of movement even when the biasing member 238 is within the opening 234. However, once the resorbing member 230 resorbs, the biasing member 238 can move out of the opening 234, and the bearing 224 can move within a comparatively larger second range of movement relative to the second prosthetic member 220.


Referring now to FIGS. 7-8B, further exemplary embodiments of the prosthetic device 310 are illustrated. Components that are similar to those of the embodiments of FIGS. 1-4B are indicated with similar reference numbers, increased by 300.


As shown, the opening 334 (e.g., recess) of the bearing 324 can be a slot that extends in the posterior-anterior direction as represented by the vertical, double headed arrow in FIG. 7. Moreover, the through hole 335 of the bearing 324 can be a slot that extends in the posterior-anterior direction. The through hole 335 can be longer than the opening 334.


Also, as shown in FIG. 8A, the resorbing member 330 can be fixed to tray 323. The resorbing member 330 can project away from the tray 323 to be received in the opening 334. The resorbing member 330 can be smaller than the opening 334. As such, the resorbing member 330 can limit movement of the bearing 324 relative to the tray 323 to within a first range A of linear movement in the posterior-anterior direction, and rotation of the bearing 324 relative to the tray 323 can be substantially eliminated by the resorbing member 330 as shown in FIG. 7. Thus, a first degree of freedom is present (i.e., anterior-posterior movement) and a second degree of freedom (i.e., rotation) is restrained. However, as shown in FIG. 8B, once the resorbing member 330 resorbs, the bearing 324 can move relative to the tray 323 over a larger range of motion. More specifically, the resorbing member 330 no longer limits movement of the bearing 324, and the bearing 324 can move relative to the tray 323 within a second range B of linear movement (FIG. 7) in the posterior-anterior direction. Also, the bearing 324 can also rotate about the guide post 333 once the resorbing member 330 resorbs. As such, the bearing 324 has multiple degrees of freedom (i.e., anterior-posterior and rotational movement). Furthermore, abutment between the guide post 333 and the through hole 335 can limit anterior-posterior and rotational movement of the bearing 324 relative to the tray 323.


Similarly, as shown in FIG. 9, the through hole 434 in the bearing 424 can be substantially the same size as the guide post 430. Also, the through hole 434 in the bearing 424 can be a slot that curves about the axis of the guide post 430. Furthermore, the tray 423 can include a projection 450 that extends in a superior direction to be received in the through hole 434. The projection 450 can be wedge shaped. Also, resorbing members 430a, 430b can be fixed to opposite sides of the projection 450. As such, abutment between the resorbing members 430a, 430b and the inner surface of the through hole 434 can limit rotational movement of the bearing 424 about the guide post 430 within a first rotational range of motion A′. However, once the resorbing members 430a, 430b resorb, abutment between the projection 450 and the inner surface of the through hole 434 can limit rotational movement of the bearing 424 about the guide post 430 within a larger second rotational range of motion B′.


It will be appreciated that in the embodiments of FIGS. 7-9, the resorbing members 330, 430a, 430b could be fixed to the bearing 324, 424. As such, the second prosthetic members 320, 420 could receive the resorbing members 330, 430a, 430b in order to limit the relative movement of the bearing 324, 424 and the second prosthetic members 320, 420 within the first range of motion A, A′.


Referring now to FIG. 10, further exemplary embodiments of the prosthetic device 510 are illustrated. Components that are similar to those of the embodiments of FIGS. 1-4B are indicated with similar reference numbers, increased by 500.


As shown, the bearing 524 can include a base post 552 that extends in an inferior direction to be received in an opening 554 of the second prosthetic member 520. The base post 552 and the opening 554 can both be tapered and can have a substantially similar size. Furthermore, the base post 552 can include a through hole 558 that extends transverse to the axis C. Likewise the post 525 of the second prosthetic member 520 can include a through hole 556 that aligns with the through hole 558.


The resorbing member 530 can be received in both through holes 556, 558 to substantially fix the bearing 524 against rotation about the axis C relative to the second prosthetic member 520. Thus, the resorbing member 530 can be considered a resorbable fastener. Once the resorbing member 530 resorbs, the bearing 524 can rotate about the axis C relative to the second prosthetic member 520. Accordingly, the initial, first range of movement of the bearing 524 relative to the second prosthetic member 520 can be substantially equal to zero, and the eventual, second range of movement of the bearing 524 relative to the second prosthetic member 520 can be greater than zero.


In other embodiments, the resorbing member 530 can initially fix the bearing 524 to the second prosthetic member 520. Over time, the resorbing member 530 can only partially resorb, and at a certain time after resorption, the resorbing member 530 can weaken and fracture due to forces transferred between the bearing 524 and the second prosthetic member 520. Once the resorbing member 530 fractures, the bearing 524 and the second prosthetic member 520 can move relative to each other over the second range of movement.


It will be appreciated that the resorbing member 30-530 can limit movement of only a portion of the bearing 24-524 relative to the second prosthetic member 20-520. As such, after resorbing, that portion of the bearing 24-524 can move relative to the second prosthetic member 20-520 while other portions of the bearing 24-524 remain limited against such relative movement.


Furthermore, as discussed above, the resorbing member 30-530 can initially (e.g., immediately after implantation) limit movement of the bearing 24-524 relative to the second prosthetic member 20-520. The resorbing member 30-530 can fix the bearing 24-524 to the second prosthetic member 20-520 or can allow relative movement within a first range of movement. Limiting movement in this way can promote healing of soft tissue, etc. Eventually (e.g., well after surgery and after healing has occurred) the resorbing member 30-530 can resorb, thereby allowing the bearing 24-524 to move relative to the second prosthetic member 20-520 over a larger, second range of movement without the need for surgical intervention. This can allow for improved mobility of the joint 14.


Moreover, the foregoing discussion discloses and describes merely exemplary embodiments of the present disclosure. One skilled in the art will readily recognize from such discussion, and from the accompanying drawings and claims, that various changes, modifications and variations may be made therein without departing from the spirit and scope of the disclosure as defined in the following claims. For instance, the sequence of the blocks of the method described herein can be changed without departing from the scope of the present disclosure.

Claims
  • 1. A prosthetic device for an anatomical feature comprising: a prosthetic member configured to be attached to the anatomical feature;a bearing having a bearing surface configured to support an articulating surface for articulation thereon; anda resorbable member sized and shaped to restrict a first degree of freedom of movement between the bearing and the prosthetic member to a range, and prevent a second degree of freedom of movement between the bearing and the prosthetic member.
  • 2. The prosthetic device of claim 1, wherein the resorbable member is constructed of a material that resorbs over time to allow for increased movement of the bearing relative to the prosthetic member after resorbtion.
  • 3. The prosthetic device of claim 1, wherein at least one of the prosthetic member and the bearing defines an opening, the resorbable element being at least partially in the opening.
  • 4. The prosthetic device of claim 3, wherein the bearing defines the opening and the resorbable member is fixed to the prosthetic member and extends away from the prosthetic member into the opening in the bearing.
  • 5. The prosthetic device of claim 1, wherein the resorbable member is sized and shaped to restrict rotation of the bearing relative to the prosthetic member.
  • 6. The prosthetic device of claim 1, wherein the prosthetic member is a tibial prosthetic member having a superiorly extending guide post and the bearing defines a through hole sized and shaped to receive the superiorly extending guide post of the tibial prosthetic member.
  • 7. The prosthetic device of claim 6, wherein the prosthetic member is a femoral prosthetic member.
  • 8. The prosthetic device claim 6, wherein the bearing defines an elongated slot and the resorbable member extends from the tibial prosthetic member into the elongated slot.
  • 9. A prosthetic device for an anatomical feature comprising: a tibial prosthetic member having a tibial tray and a guide post extending from the tibial tray;a femoral prosthetic member, the femoral prosthetic member having portions defining an articulating surface;a bearing having a bearing surface configured to support the articulating surface for articulation thereon, the bearing defining an elongated bore extending along a longitudinal axis and configured to receive the guide post and defining an elongated opening extending along the longitudinal axis; anda resorbable member extending into the elongated opening, the resorbing member sized and shaped to restrict movement of the bearing member relative to the tibial prosthetic member.
  • 10. The prosthetic device of claim 9, wherein the resorbable member comprises a resorbable material that resorbs over time to allow for increased movement of the bearing relative to the tibial prosthetic member after resorption.
  • 11. The prosthetic device of claim 9, wherein the resorbable member is sized and shaped to restrict a linear movement of the bearing member relative to the tibial prosthetic member to a range, and the resorbable member is sized and shaped to prevent rotational movement of the bearing member relative to the tibial prosthetic member.
  • 12. The prosthetic device of claim 9, wherein the resorbable member restricts movement of the bearing in a substantially anterior-posterior direction relative to the tibial prosthetic member.
  • 13. The prosthetic device of claim 9, wherein the resorbable member restricts rotational movement of the bearing relative to the tibial prosthetic member.
  • 14. A prosthetic device for an anatomical feature comprising: a femoral prosthetic member configured to be attached to a femur and having an articulating surface;a tibial prosthetic member configured to be attached to a tibia;a bearing having a bearing surface configured to support the articulating surface of the femoral prosthetic member for articulation thereon; anda resorbable member that restricts movement of the bearing member relative to the tibial prosthetic member, wherein the bearing is sized and shaped to allow a first degree of freedom of movement of the tibial prosthetic member relative to the bearing and a second degree of freedom of movement of the tibial prosthetic member relative to the bearing, and the resorbable member is sized and shaped to restrict the second degree of freedom of movement.
  • 15. The prosthetic device of claim 14, wherein the resorbable member comprises a resorbable material that resorbs over time to allow for increased movement of the bearing relative to the tibial prosthetic member after resorption.
  • 16. The prosthetic device of claim 14, wherein the first degree of freedom of movement is linear movement and the second degree of freedom of movement is rotational movement.
  • 17. The prosthetic device of claim 14, wherein, with respect to the first degree of freedom of movement, the bearing is sized and shaped to allow movement of the tibial prosthetic member over a second range of movement relative to the bearing, and the resorbable member is sized and shaped to restrict movement of the tibial prosthetic member to a first range relative to the bearing, the second range being larger than the first range.
  • 18. The prosthetic device of claim 14, wherein the resorbable member is fixed to the tibial prosthetic member and extends away from the tibial prosthetic member into a recess in the bearing.
  • 19. The prosthetic device of claim 14, wherein the resorbable member is sized and shape to prevent movement of the tibial prosthetic member relative to the bearing in the second degree of freedom of movement, and the resorbable member is sized and shaped to restrict movement of the tibial prosthetic member relative to the bearing to a range in the first degree of freedom of movement.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 13/674,540 filed on Nov. 12, 2012, which is a divisional of U.S. patent application Ser. No. 12/708,755 filed on Feb. 19, 2012, now U.S. Pat. No. 8,308,808 issued on Nov. 13, 2012. The entire disclosure of the above application is incorporated herein by reference.

US Referenced Citations (169)
Number Name Date Kind
3728742 Averill et al. Apr 1973 A
3748662 Helfet Jul 1973 A
3774244 Walker Nov 1973 A
3869729 Attenborough Mar 1975 A
3958278 Lee et al. May 1976 A
3964106 Hutter, Jr. et al. Jun 1976 A
3996624 Noiles Dec 1976 A
4081866 Upshaw et al. Apr 1978 A
4085466 Goodfellow et al. Apr 1978 A
4094017 Matthews et al. Jun 1978 A
4136405 Pastrick et al. Jan 1979 A
4205400 Shen et al. Jun 1980 A
4207627 Cloutier Jun 1980 A
4209861 Walker et al. Jul 1980 A
4213209 Insall et al. Jul 1980 A
4215439 Gold et al. Aug 1980 A
4216549 Hillberry et al. Aug 1980 A
4219893 Noiles Sep 1980 A
4224696 Murray et al. Sep 1980 A
4224697 Murray et al. Sep 1980 A
4242759 White Jan 1981 A
4249270 Bahler et al. Feb 1981 A
4257129 Volz Mar 1981 A
4285070 Averill Aug 1981 A
4298992 Burstein et al. Nov 1981 A
4301553 Noiles Nov 1981 A
4309778 Buechel et al. Jan 1982 A
4340978 Buechel et al. Jul 1982 A
4462120 Rambert et al. Jul 1984 A
4470158 Pappas et al. Sep 1984 A
4538305 Engelbrecht et al. Sep 1985 A
4568348 Johnson et al. Feb 1986 A
4586933 Shoji et al. May 1986 A
4634444 Noiles Jan 1987 A
4637382 Walker Jan 1987 A
4673407 Martin Jun 1987 A
4711639 Grundei Dec 1987 A
4714474 Brooks, Jr. et al. Dec 1987 A
4728332 Albrektsson Mar 1988 A
4790853 Engelbrecht et al. Dec 1988 A
4808185 Penenberg et al. Feb 1989 A
4822362 Walker et al. Apr 1989 A
4822365 Walker et al. Apr 1989 A
4865607 Witzel et al. Sep 1989 A
4883488 Bloebaum et al. Nov 1989 A
4888021 Forte et al. Dec 1989 A
4892547 Brown Jan 1990 A
4911721 Andergaten 3 et al. Mar 1990 A
4950297 Elloy et al. Aug 1990 A
4950298 Gustilo et al. Aug 1990 A
4959071 Brown et al. Sep 1990 A
4997445 Hodorek Mar 1991 A
5007933 Sidebotham et al. Apr 1991 A
5011496 Forte et al. Apr 1991 A
5037439 Albrektsson et al. Aug 1991 A
5047057 Lawes Sep 1991 A
5064437 Stock et al. Nov 1991 A
5071438 Jones et al. Dec 1991 A
5080675 Lawes et al. Jan 1992 A
5092895 Albrektsson et al. Mar 1992 A
5116375 Hofmann May 1992 A
5116376 May May 1992 A
5133758 Hollister Jul 1992 A
5139521 Schelhas Aug 1992 A
5147405 Van Zile et al. Sep 1992 A
5147406 Houston et al. Sep 1992 A
5171283 Pappas et al. Dec 1992 A
5176710 Hahn et al. Jan 1993 A
5181925 Houston et al. Jan 1993 A
5197987 Koch et al. Mar 1993 A
5201881 Evans Apr 1993 A
5219362 Tuke et al. Jun 1993 A
5226916 Goodfellow et al. Jul 1993 A
5236461 Forte Aug 1993 A
5271747 Wagner et al. Dec 1993 A
5282868 Bahler Feb 1994 A
5282870 Moser et al. Feb 1994 A
5314482 Goodfellow et al. May 1994 A
5314483 Wehrli et al. May 1994 A
5330532 Ranawat Jul 1994 A
5330533 Walker et al. Jul 1994 A
5330534 Herrington et al. Jul 1994 A
5358527 Forte Oct 1994 A
5358529 Davidson Oct 1994 A
5358530 Hodorek Oct 1994 A
5358531 Goodfellow et al. Oct 1994 A
5370699 Hood et al. Dec 1994 A
5370700 Sarkisian et al. Dec 1994 A
5370701 Finn Dec 1994 A
5387240 Pottenger et al. Feb 1995 A
5395401 Bahler Mar 1995 A
5405394 Davidson Apr 1995 A
5405395 Coates Apr 1995 A
5405396 Heldreth et al. Apr 1995 A
5413604 Hodge May 1995 A
5413608 Keller May 1995 A
5466530 England et al. Nov 1995 A
5480446 Goodfellow et al. Jan 1996 A
5514183 Epstein et al. May 1996 A
5549686 Johnson et al. Aug 1996 A
5549689 Epstein et al. Aug 1996 A
5549690 Hollister et al. Aug 1996 A
5556432 Kubein-Meesenburg et al. Sep 1996 A
5571197 Insall Nov 1996 A
5609639 Walker et al. Mar 1997 A
5609643 Colleran et al. Mar 1997 A
5609645 Vinciguerra Mar 1997 A
5639279 Burkinshaw et al. Jun 1997 A
5641323 Caldarise Jun 1997 A
5658342 Draganich et al. Aug 1997 A
5658344 Hurlburt Aug 1997 A
5662158 Caldarise Sep 1997 A
5683467 Pappas Nov 1997 A
5683468 Pappas Nov 1997 A
5702458 Burstein et al. Dec 1997 A
5702466 Pappas et al. Dec 1997 A
5725584 Walker et al. Mar 1998 A
5755801 Walker et al. May 1998 A
5755802 Gerber May 1998 A
5755804 Schmotzer et al. May 1998 A
5800552 Forte Sep 1998 A
5824096 Pappas et al. Oct 1998 A
5824100 Kester et al. Oct 1998 A
5824102 Buscayret Oct 1998 A
5824103 Williams Oct 1998 A
5871542 Goodfellow et al. Feb 1999 A
5871545 Goodfellow et al. Feb 1999 A
5871546 Colleran et al. Feb 1999 A
5879387 Jones et al. Mar 1999 A
5879392 McMinn Mar 1999 A
5879394 Ashby et al. Mar 1999 A
5906643 Walker May 1999 A
5997577 Herrington et al. Dec 1999 A
6004352 Buni Dec 1999 A
6019794 Walker Feb 2000 A
6039764 Pottenger et al. Mar 2000 A
6068658 Insall et al. May 2000 A
6080195 Colleran et al. Jun 2000 A
6090144 Letot et al. Jul 2000 A
6099570 Livet et al. Aug 2000 A
6117175 Bosredon Sep 2000 A
6123729 Insall et al. Sep 2000 A
6152960 Pappas Nov 2000 A
6162254 Timoteo Dec 2000 A
6165223 Metzger et al. Dec 2000 A
6203576 Afriat et al. Mar 2001 B1
6210444 Webster et al. Apr 2001 B1
6210445 Zawadzki Apr 2001 B1
6217618 Hileman Apr 2001 B1
6296666 Gardner Oct 2001 B1
6413279 Metzger et al. Jul 2002 B1
6485519 Meyers et al. Nov 2002 B2
6660039 Evans et al. Dec 2003 B1
6923833 Wasielewski Aug 2005 B2
6972039 Metzger et al. Dec 2005 B2
6986791 Metzger Jan 2006 B1
7871442 Servidio Jan 2011 B2
8308808 Hershberger Nov 2012 B2
8986391 Hershberger Mar 2015 B2
20050107886 Crabtree et al. May 2005 A1
20050216091 Wasielewski Sep 2005 A1
20070100463 Aram et al. May 2007 A1
20070162143 Wasielewski Jul 2007 A1
20070162144 Wasielewski Jul 2007 A1
20080091272 Aram et al. Apr 2008 A1
20090125116 Crabtree et al. May 2009 A1
20090318976 Gabriel et al. Dec 2009 A1
20110208316 Hershberger Aug 2011 A1
20130173009 Hershberger Jul 2013 A1
Foreign Referenced Citations (30)
Number Date Country
2802568 Jul 1979 DE
3529894 Mar 1987 DE
4009360 Aug 1991 DE
0186471 Jul 1986 EP
0327297 Aug 1989 EP
0346183 Dec 1989 EP
0349173 Jan 1990 EP
0381352 Aug 1990 EP
0442330 Aug 1991 EP
0498586 Aug 1992 EP
0510178 Oct 1992 EP
0510299 Oct 1992 EP
0519873 Dec 1992 EP
0592750 Apr 1994 EP
0627203 Dec 1994 EP
653927 May 1995 EP
0970667 Jan 2000 EP
2663536 Dec 1991 FR
2685632 Jul 1993 FR
2758456 Jul 1998 FR
1534263 Nov 1978 GB
2219942 Dec 1989 GB
2296443 Jul 1996 GB
2313314 Nov 1997 GB
WO-9203108 Mar 1992 WO
WO-9208424 May 1992 WO
WO-9426212 Nov 1994 WO
WO-9603097 Feb 1996 WO
WO-9624311 Aug 1996 WO
WO-9802116 Jan 1998 WO
Non-Patent Literature Citations (25)
Entry
“AGC, Total Knee System, Intramedullary with Distractor Surgical Technique,” brochure, Biomet, Inc. Jan. 1989.
“AGC, Total Knee System, Surgical Overview featuring Accu-Line TM Knee Instrumentation,” brochure, Biomet, Inc. Jun. 1991.
“AGC, Total Knee System, Tradition Series,” brochure, Biomet, Inc. Jun. 1995.
“AGC, Total Knee System, Unicondylar Surgical Overview,” brochure, Biomet, Inc. Jan. 1989.
“Maxim, The Complete Knee System,” brochure, Biomet, Inc. Jun. 1995.
“Regenerex® Tibial Cone Augment, Surgical Technique Addendum to the Vanguard® SSK Revision System,” brochure. Biomet® Orthopedics. (2009) pp. 1-8 (12 sheets).
“Signature™ Personalized Patient Care, Surgical Technique Addendum to the Vanguard Knee System” brochure. Biomet® Orthopedics, Inc. (2009) pp. 1-8.
“The Oxford® Partial Knee—Surgical Technique” Biomet Orthopedics, 2009.
“The Profix Total Knee System,” brochure/advertisement. Smith & Nephew,1999, 2 sheets.
“Trac Mobile Bearing Knee System, Two Radius Area Contact Posterior Stabilized Mobile Bearing Knee System Surgical Technique” brochure . (1999) 32 sheets.
“Vanguard Complete Knee System, Cruciate Retaining,” brochure (6 pages) 2007. Biomet Orthopedics, Inc.
“Vanguard Complete Knee System, System Summary,” brochure, (4 sheets) 2007. Biomet Orthopedics, Inc.
“Vanguard™ Complete Knee System SSK Revision System,” brochure. Biomet Orthopedics, Inc. 2007.
“Vanguard® PFR Partial Knee Patellofemoral Replacement System,” Surgical Technique brochure. Biomet Orthopaedics, (2010) pp. 1-25.
Aglietti, P., et al., “Total Knee Replacement—Problems Related to the Posterior Cruciate Ligament and Fixed Versus Mobile Bearings,” European Federation of National Associations of Orthopaedics and Traumatology, (1997) pp. 15-24.
Churchill, D. L., et al. “The Transepicondylar Axis Approximates the Optimal Flexion Axis of the Knee,” Clinical Orthopaedics and Related Research (Nov. 1998) No. 356, pp. 111-118.
Kocmond, J. H., et al. “Stability and Range of Motion of Insall-Burstein Condylar Prostheses”, The Journal of Arthroplasty, (1995) vol. 10, No. 3 , pp. 383-388.
Kurosawa, H., et al., “Geometry and Motion of the Knee for Implant and Orthotic Design,” J. Biomechanics (1985) vol. 18, No. 7, pp. 487-499.
Markolf, Keith L., et al. “The Role of Joint Load in Knee Stability,” Journal of Bone and Joint Surgery, Incorporated (Apr. 1981) vol. 63-A, No. 4 pp. 570-585.
Menchetti, Paolo, M., et al. “Mechanical Evaluation of Mobile Bearing Knees.” The American Journal of Knee Surgery, (Spring 1997) vol. 10, No. 2, pp. 73-82.
Microplasty™ minimally invasive knee instruments brochure, Surgical Technique for the Maxim®, Ascent™ and Vanguard™ Total Knee Systems, Biomet Orthopedics, Inc., Feb. 29, 2004.
Schipplein, O.D., et al. “Interaction Between Active and Passive Knee Stabilizers During Level Walking,” Journal of Orthopaedic Research (1991) vol. 9, No. 1, pp. 113-119.
Vanguard™ SSK Revision System—Surgical Technique, Biomet® Orthopedics, 2008.
Vanguard® SSK Revision System, 2009.
Walker, P.S., et al., “Controlling the Motion of Total Knee Replacements using Intercondylar Guide Surfaces,” Journal of Orthopedic Research (2000) vol. 18, pp. 48-55.
Related Publications (1)
Number Date Country
20150320566 A1 Nov 2015 US
Divisions (1)
Number Date Country
Parent 12708755 Feb 2010 US
Child 13674540 US
Continuations (1)
Number Date Country
Parent 13674540 Nov 2012 US
Child 14664116 US