The present patent application relates to orthopedic prostheses, and more particularly, to a tool and methods for assembling a modular prosthesis.
A joint arthroplasty procedure may be performed to repair or replace damaged bone of a patient's joint, such as bone that is damaged due to a traumatic injury or a degenerative illness. For example, during a total elbow arthroplasty procedure, the surgeon implants a prosthetic humeral component into the distal end of a patient's humerus and a prosthetic ulnar component into the proximal end of the patient's ulna. The prosthetic humeral component and the prosthetic ulnar component are generally joined by a hinge that enables pivoting movement between the prosthetic humeral component and the prosthetic ulnar component, to recreate the natural, anatomical articulation of the elbow joint.
Orthopedic prostheses, such as the above-mentioned elbow prosthesis having a humeral component and an ulnar component, can be modular and one or both of the components can have a plurality of individual pieces. In some cases, assembling the components and the prosthesis can be difficult given, for example, the complexity of the design and/or a small size of the components and pieces.
The present inventors recognize, among other things, an opportunity for an assembly tool that aids in assembling a modular prosthesis and/or a component of the prosthesis. The assembly tool described herein can be used, for example, in a joint arthroplasty procedure or in a revision procedure.
To better illustrate the assembly tool and methods disclosed herein, the following non-limiting examples are provided:
In an example, an assembly tool for assembling components of an implant comprises a finger assembly, a handle assembly, and a crossbar assembly connected to the finger assembly and the handle assembly. The finger assembly can comprise a first finger sized and shaped to releasably engage a first component of the implant and a second finger sized and shaped to releasably engage a second component of the implant, the first and second fingers oriented substantially parallel to each other. The handle assembly can comprise a first handle pivotally connected to a second handle, the handle assembly configured to control movement of the first and second fingers when the first and second handles are actuated. The crossbar assembly can be configured to maintain the first and second fingers substantially parallel to each other during movement of the first and second fingers by actuation of the first and second handles.
In an example, an assembly tool for assembling a multi-component implant comprises a first finger including a first attachment feature configured to releasably secure a first component of the implant to the first finger and a second finger including a second attachment feature configured to releasably secure a second component of the implant to the second finger, wherein the first and second fingers are oriented substantially parallel to each other. The assembly tool further comprises a handle assembly comprising a first handle pivotally connected to a second handle, the handle assembly configured to control movement of the first and second fingers when the first and second handles are actuated. The assembly tool further comprises a first finger extension extending from the first finger and connected to the second handle, a second finger extension extending from the second finger and connected to the first handle, and a crossbar assembly comprising a first crossbar pivotally connected to a second crossbar. The crossbar assembly can be configured to maintain the first and second fingers substantially parallel to each other throughout movement of the first and second fingers by actuation of the first and second handles.
In an example, a method of assembling a multi-component implant using an assembly tool comprises mounting a first component of the implant onto a first finger of the assembly tool such that the first finger releasably engages the first component to the assembly tool and mounting a second component of the implant onto a second finger of the assembly tool such that the second finger releasably engages the second component to the assembly tool. The method further comprises moving the first and second fingers towards each other and into a compressed position to attach the first component to the second component, maintaining a substantially parallel relationship between the first and second fingers throughout movement of the first and second fingers, and releasing the first and second fingers from the compressed position back to a relaxed position.
This overview is intended to provide a summary of subject matter of the present patent application. It is not intended to provide an exclusive or exhaustive explanation of the invention. The detailed description is included to provide further information about the present patent application.
In the drawings, which are not necessarily drawn to scale, like numerals may describe similar components in different views. Like numerals having different letter suffixes may represent different instances of similar components. The drawings illustrate generally, by way of example, but not by way of limitation, various embodiments discussed in the present document.
The present application relates to devices and methods for an assembly tool that can be used before or during an orthopedic procedure involving a prosthesis. The assembly tool can be used to aid in assembling all or a portion of the prosthesis.
For illustrative purposes,
The elbow prosthesis 100, as shown in
With reference to
The ulnar component 104 can include an ulnar stem 130, an ulnar head 132 having an aperture or opening 134 extending through the ulnar head 132, and an ulnar neck 131 between the head 132 and the stem 130. The ulnar head 132 can also be referred to as an ulnar eye.
Each of the first 108 and second 110 ulnar bearings can extend into the aperture 134 of the ulnar head 132. The pin 116 can extend through the first ulnar bearing 108, the ulnar head 132, and the second ulnar bearing 110. Opposing end portions of the pin 116 can extend into the first 124 and second 126 ears of the yoke 122 of the humeral component 102. When assembled to the humeral component 102, the pin 116 can define an axis upon which the ulnar component 104 can pivot relative to the humeral component 102.
The first fastener 112 can extend into the first ear 124 of the yoke 122 and the second fastener 114 can extend into the second ear 126 of the yoke 122 to secure the humeral 102 and ulnar 104 components to each other. In an example, the first 112 and second 114 fasteners can be a first screw and a second screw, respectively. The engagement between the first fastener 112, the first ear 124, and the pin 116, as well as a similar engagement between the second fastener 114, the second ear 126, and the pin 116, is described in further detail below.
When the humeral component 102 and the ulnar component 104 are implanted into a humerus and an ulna, respectively, of a patient, the yoke 122 of the humeral component 102 and the ulnar head 132 of the ulnar component 104 can remain exposed. The ulnar head 132 can be configured to pivot about the pin 116 to enable movement of the ulnar component 104 relative to the humeral component 102, as described above.
The pin 116 can be made of one or more materials suitable for implantation within a human or animal body and for enabling pivoting movement of one component relative to another component. These materials can include, but are not limited to, stainless steel, titanium, cobalt, or one or more alloys thereof. In an example, the pin 116 can be cobalt chrome.
The first ulnar bearing 108 can include a first opening or hole 204 for receiving the pin 116. In an example, the first hole 204 can include a chamfer 206 to help lead the pin 116 through the first hole 204. The pin 116 can have a press fit with the first and second ulnar bearings 108 and 110.
The first ulnar bearing 108 can include a first bearing extension 208 having an articulation surface 210 and an end face 212. A second opening or hole 214 can extend through the end face 212 for receiving the pin 116. In an example, the second hole 214 can include a chamfer 216 to help lead the pin 116 through the second hole 216. A compression rib 218 can extend from the end face 212 on at least a portion of the end face 212. The first 204 and second 214 holes can converge within the first ulnar bearing 108 so as to form a single continuous channel that is structured to allow passage of the pin 116.
In an example, the second ulnar bearing 110 can be substantially similar to the first ulnar bearing 108. When rotated by approximately 180 degrees relative to the position in
The humeral bearing 106 and/or the first 108 and second 110 ulnar bearings can be made of one or more materials suitable for implantation within a human or animal body. In an example, the humeral bearing 106 and/or the first 108 and second ulnar bearings 110 can be made of an elastomeric material, such as, for example, a ultrahigh molecular weight polyethylene (UHMWPE). In an example, the humeral bearing 106 can be formed from a crosslinked ultrahigh molecular weight polyethylene blend stabilized with Vitamin E, such as disclosed in U.S. Pat. No. 7,846,376. In an example, the first 108 and second 110 ulnar bearings can be formed from a crosslinked ultrahigh molecular weight polyethylene blend stabilized with Vitamin E, such as disclosed in U.S. Pat. No. 7,846,376. When formed from an elastomeric material, the bearings 106, 108 and 110 can be squeezed or compressed, for example to overcome an interference fit or press fit, and/or conform to a surrounding metal component.
A next step in the assembly of the elbow prosthesis 100 can include connecting the ulnar component 104 to the humeral component 102, which can include placing the first end portion 176 of the pin 116 into the first ear 124 of the yoke 122 and placing the second end portion 178 of the pin 116 into the second ear 126 of the yoke 122. The pin 116 and the first 124 and second 126 ears of the yoke 122 are each configured such that the first end portion 176 of the pin 116 can be secured inside the opening 146 formed in the first ear 124 and the second end portion 178 of the pin 116 can be secured inside the opening 154 formed in the second ear 126.
As described above, the first 108 and second 110 ulnar bearings can be formed of one or more elastomeric or compressible materials such the first 108 and second 110 ulnar bearings can be squeezed or compressed together as the bearing assembly 230 and the ulnar component 104 are assembled onto the humeral component 102. In an example, when the first 108 and second 110 ulnar bearings are squeezed together, the compression rib 218 on the first ulnar bearing 108 (see
Once the ulnar bearing assembly 230 is attached to the humeral component 102, the first 108 and second 110 ulnar bearings can be secured within the yoke 122. In an example, the external face 196 of the first ulnar bearing 108 (see
A next step in the assembly of the elbow prosthesis 100 can include inserting the first fastener 112 through the bore 150 of the first ear 124 and inserting the second fastener 114 through the bore 152 of the second ear 126. Once the assembly is complete, the ulnar component 104 can pivot about the pin 116 such as to provide pivotal movement of the ulnar component 104 relative to the humeral component 102. As the ulnar component 104 moves, the ulnar head 132 can articulate against the articulation surface 182 of the humeral bearing 106.
The assembly of the elbow prosthesis 100 can be configured such that the bearings 106, 108 and 110, or at least one feature on the bearings 106, 108 and 110, can compress during an assembly of the elbow prosthesis 100 and then relax and conform to a surrounding area. Various features on the ulnar bearings 108 and 110, such as the tabs described above, or features on the humeral bearing 106 can allow an interference fit or press fit that can result in a stable placement of the bearings in the elbow prosthesis 100, such as to reduce or eliminate any movement of the bearings 106, 108, and 110 within the elbow prosthesis 100, particularly as various forces or loads are placed on the bearings 106, 108, and 110. In certain examples, alternative or additional features to those described herein can be used on the bearings 106, 108, 110 to provide a press fit.
The elbow prosthesis 100 is an example of a modular prosthesis having a plurality of components that can be assembled together. The assembly of the elbow prosthesis 100 can take place outside of the patient's body, or some or all of the assembly can take place after the ulnar 104 and/or humeral 102 components have been inserted into the ulnar and humeral medullary canals, respectively. The ulnar component 104, once assembled, can include the bearing assembly 230 and the pin 116. As described above, the first 108 and second 110 ulnar bearings of the bearing assembly 230 can include features to create an interference fit between the first 108 and second 110 bearings; moreover, the pin 116 and the first 108 and second 110 bearings can each be sized, shaped and configured to create a press fit between the pin 116 and the first 108 and second 110 bearings. The sizes of these components of the elbow prosthesis 100 can be small, and, for at least this reason, it can be difficult to assemble the bearing assembly 230 onto the ulnar component 104.
Described herein is an example of an assembly tool that can be used for assembling the bearing assembly 230 onto the ulnar component 104 of the elbow prosthesis 100 described above. Although the assembly tool is described for use in assembling components of an elbow prosthesis, the assembly tool described herein can similarly be used for other types of prostheses.
The finger assembly 304 can be sized, shaped, and configured to engage components of the ulnar bearing assembly 230 shown in
The assembly tool 300 can be configured such that the first 312 and second 316 fingers, including the first 314 and second 318 finger extensions, remain substantially parallel to each other throughout movement of the first 312 and second 316 fingers by the first 308 and second 310 handles. The crossbar assembly 306 can be sized, shaped and configured to maintain the first 312 and second 316 fingers in a substantially parallel orientation relative to each other.
As shown in
The bottom portion 338 of the first finger extension 314 can include a slot 352 that a pin 353 can extend through to connect the second crossbar 322 to the first finger extension 314. Similarly, the bottom portion 334 of the second finger extension 318 can include a slot 354 that a pin 355 can extend through to connect the first crossbar 320 to the second finger extension 318. The slots 352 and 354 can facilitate vertical movement of the pins 353 and 355, respectively, in response to movement of the finger assembly 304 by the handle assembly 302, as described further below.
The first 314 and second 318 finger extensions can include a first gage portion 356 and a second gage portion 358, respectively, which can extend from the bottom portions 338 and 334 of the finger extensions 314 and 318, respectively. The gage portions 356 and 358 are discussed in further detail below in reference to
The finger assembly 304 can include the first 324 and second 326 guide pins, which can each extend between the first 312 and second 316 fingers. Each of the guide pins 324 and 326 can be received in an aperture near a bottom portion of the corresponding first 312 and second 316 fingers. A first end of the first guide pin 324 can be received in and extend through a first aperture 360 in the first finger 312 and a first end of the second guide pin 326 can be received in and extend through a second aperture 362 in the first finger 312. A second end of the first guide pin 324 can be received in a first aperture in the second finger 316 and a second end of the second guide pin 326 can be received in a second aperture in the second finger 316.
In an example, the first 360 and second 362 apertures of the first finger 312 can extend through the first finger 312 such that the guide pins 324 and 326 can extend through an outside of the first finger 312 (as shown in
A first spring 364 can be wrapped around the first guide pin 324 and a second spring 366 can be wrapped around the second guide pin 326. When the first 312 and second 316 fingers are moved toward each other, by way of the handles 308 and 310, the springs 364 and 366 can compress. As the fingers 312 and 316 are brought closer together, a greater portion of the guide pins 324 and 326 can extend through the first 360 and second 362 apertures in the first finger 312 (see
A user can grasp and squeeze the handles 308 and 310 in order to actuate or move the handles 308 and 310 towards each other, as shown in
As the handles 308 and 310 move towards each other, the top portions 368 and 372 of the first 320 and second 322 crossbars, respectively, can be configured to move towards each other. Similarly, as the handles 308 and 310 move away from each other and return to a relaxed position, the top portions 368 and 372 can be configured to move away from each other. When the top portions 368 and 372 move towards (or away) from each other, the bottom portions 370 and 374 of the first 320 and second 322 crossbars, respectively, also move towards (or away) from each other in a substantially equal amount. Throughout movement of the handles 308 and 310, a distance D1 between the top portions 368 and 372 can be substantially the same as a distance D2 between the bottom portions 370 and 374.
A distance between the top portion 368 of the first crossbar 320 and the bottom portion 374 portion of the second crossbar 322 can be defined as a distance D3. A distance between the top portion 372 of the second crossbar 322 and the bottom portion 370 of the first crossbar 320 can be defined as a distance D4. Similar to the distances D1 and D2 being substantially equal to each other, the distances D3 and D4 can be substantially equal to each other throughout movement of the handles 308 and 310.
As the handles 308 and 310 move towards each other, the distances D1 and D2 decrease. Reducing the distances D1 and D2 can result in increasing the distances D3 and D4. To accommodate an increase in the distances D3 and D4, the first 314 and second 318 finger extensions can include the slots 352 and 354, respectively, which can permit the bottom portions 370 and 374 of the first 320 and second 322 crossbars, respectively, to generally travel in a vertical direction (V1) in response to a decrease or increase in the distances D3 and D4.
Because each of the first 314 and second 318 finger extensions can be connected to the crossbar assembly 306, movement of the first 320 and second 322 crossbars can result in movement of the first 312 and second 316 fingers towards and away from each other. The use of the crossbars 320 and 322 and the slots 352 and 354 in the first 314 and second 318 finger extensions, respectively, can maintain the fingers 312 and 316 substantially parallel to each other throughout movement of the fingers 312 and 316.
Other crossbar designs in addition to, or as an alternative to, the crossbar assembly 306 described herein can be used as part of the assembly tool 300.
The first finger extension 314 can include the first gage portion 356 that extends from the bottom portion 338 of the first finger extension 314. The second finger extension 318 can include the second gage portion 358 that extends from the bottom portion 334 of the second finger extension 318. The first 356 and second 358 gage portions can be used in combination to form a site gage for the user of the assembly tool 300.
The first gage portion 356 can include a reference marker 376 and the second gage portion 358 can include a first marker 378 and a second marker 380. As an example, the first marker 378 can be used to designate a Size 4 implant, and the second marker 380 can be used to designate a Size 5 or a Size 6 implant. When a user has squeezed the handles 308 and 310 such that the reference marker 376 on the first gage portion 356 is aligned with the first marker 378 on the second gage portion 358, the user can confirm that the first 312 and second 316 fingers are a sufficient distant apart for assembly of the bearing assembly 230 for a Size 4 implant. Similarly, for a Size 5 or Size 6 implant, because the implant is generally larger, the ulnar component 104 and the bearing assembly 230 are also generally larger, thus the user does not have to squeeze the fingers 312 and 316 as close together during assembly. When a user has squeezed the handles 308 and 310 such that the reference marker 376 is aligned with the second marker 380 on the second gage portion 358, the fingers 312 and 316 are sufficiently close together for assembly of the bearing assembly 230 for a Size 5 or Size 6 implant. Other types of size identifiers can be used on gage portions 356 and 358 in addition to or as an alternative to the Size 4, 5 and 6 identifiers shown in
The markers 376, 378, and 380 can be etched onto the first 356 and second 358 gage portions, or the markers 376, 378, and 380 can be formed using any known method of creating a mark or notch. In an example, the second gage portion 358 can have more or less than the two markers 378 and 380 shown in
In an example, the first 312 and second 316 fingers can be substantially the same; and the first 314 and second 318 finger extensions can be substantially the same. Although the second finger 316, and its corresponding features, is described in detail in reference to
The second finger 316 and the second finger extension 318 can be connected to each other using known connection means. In an example, the second finger 316 and the second finger extension 318 can be welded together. In another example, the second finger 316 and the second finger extension 318 can be integrally formed together. The second finger 316 can include a support pin 382, a spring 384, a finger pin 386, a recess 388, an axle pin aperture 390, and an overhang 392. The finger pin 386 can be movable in a vertical direction given its connection to the spring 384, which can be stabilized by the support pin 382. The recess 388 can be configured to releasably receive a feature on the ulnar bearing 108 and releasably secure the ulnar bearing 108 to the second finger 316. More specifically, in an example, the recess 388 can be configured to releasably receive the tab 198 on the ulnar bearing 108, as discussed further below. The axle pin aperture 390 can be configured to releasably receive the pin 116, also referred to as an axle pin, of the elbow prosthesis 100, as discussed further below.
A method of assembling the bearing assembly 230 on the ulnar component 104 is illustrated below in
To releasably engage the first ulnar bearing 108 with the second finger 316, a user can place the first ulnar bearing 108 into the second finger 316 such that the tab 198 on the ulnar bearing 108 can be aligned with the recess 388. As such, a top portion 394 of the finger pin 386 can be received within the slot 199 on the first ulnar bearing 108, adjacent to the tab 198 (see
The axle pin aperture 390 on the second finger 316 can be configured to temporarily receive or hold the pin 116. The pin 116 can be manually inserted into the axle pin aperture 390 by the user. The pin 116 can have a loose to moderate engagement with the aperture 390 such that the aperture 390 can temporarily hold the pin 116 in place; thus the second finger 316 can releasably engage the pin 116. In an example, the engagement of the pin 116 with the second finger 316 can be less constrained than the above described engagement (or securement) of the ulnar bearing 108 with the second finger 316.
Other designs can be used for the first 312 and second 316 fingers in addition to, or as an alternative to, the design described above in reference to
The assembly tool 300 can be made of one or more materials suitable for use in surgical procedures for humans or animals. These materials can include, but are not limited to, stainless steel, titanium, cobalt, or one or more alloys thereof. In an example, some or all of the components of the assembly tool 300 can be made of stainless steel. In such a case, some of the components may be made of a first type of stainless steel and other components may be made of at least a second type of stainless steel. In an example, the type of material selected for a particular component can depend, in part, on whether that component articulates relative to another component.
To move the pin 116 from the first finger 312 to the second finger 316, the user can squeeze the handles 308 and 310 together until the assembly 300 is generally in the closed position (see
When the user starts to release the handles 308 and 310, the first end portion 176 of the pin 116 can release from the first finger 312 because an engagement of the first end portion 176 of the pin 116 in the aperture 410 of the first finger 312 can be weaker than the press fit securement of the second end portion 178 of the pin 116 to the first ulnar bearing 108.
In the fourth step 400d of the method 400, shown in
In a fifth step 400e, shown in
In an example, the ulnar component 104 can already be implanted inside the patient's ulnar medually canal prior to assembling the bearing assembly 230 onto the ulnar component 104. In that case, the user can have a limited amount of space to work with and/or limited to no visual access to the area around the ulnar component 104 where the bearing assembly 230 is to be mounted to the ulnar component 104. Thus, the user can rely on the site gage (see
When the fingers 312 and 316 are brought together in the fifth step 400e, the pin 116 can extend through the aperture 134 of the ulnar head 132 and the second ulnar bearing 110. The pin 116 can form a press fit with the second ulnar bearing 110. When the fingers 312 and 316 are brought together, the first bearing extension 208 of the first ulnar bearing 108 (see
Modifications can be made to the assembly tool 300 such that the assembly tool 300 can be used with other types of prostheses. For example, the fingers 312 and 316 can be modified to engage with other components in addition to or as an alternative to the components of the bearing assembly 230 as shown in the figures and described above.
The assembly tool 300 can be provided in combination with a prosthesis such that, for example, a user can have easy access to the assembly tool 300 during an implantation procedure for the prosthesis. In an example, a system and/or a kit for repairing an elbow joint of a patient can include the elbow prosthesis 100 and the assembly tool 300. In an example, the kit can include a plurality of prostheses of varying sizes and/or a plurality of components of varying sizes. The kit can include instructions for use of the assembly tool 300. In an example, the elbow prosthesis 100 and the assembly tool 300 can be separately provided to the user, but used in combination during the implant procedure. The assembly tool 300 can be reusable in a subsequent implantation procedure after undergoing sterilization.
The above detailed description includes references to the accompanying drawings, which form a part of the detailed description. The drawings show, by way of illustration, specific embodiments in which the invention can be practiced. These embodiments are also referred to herein as “examples.” Such examples can include elements in addition to those shown or described. However, the present inventors also contemplate examples in which only those elements shown or described are provided. Moreover, the present inventors also contemplate examples using any combination or permutation of those elements shown or described (or one or more aspects thereof), either with respect to a particular example (or one or more aspects thereof), or with respect to other examples (or one or more aspects thereof) shown or described herein.
In the event of inconsistent usages between this document and any documents so incorporated by reference, the usage in this document controls. In this document, the terms “a” or “an” are used, as is common in patent documents, to include one or more than one, independent of any other instances or usages of “at least one” or “one or more.” In this document, the term “or” is used to refer to a nonexclusive or, such that “A or B” includes “A but not B,” “B but not A,” and “A and B,” unless otherwise indicated. In this document, the terms “including” and “in which” are used as the plain-English equivalents of the respective terms “comprising” and “wherein.” Also, in the following claims, the terms “including” and “comprising” are open-ended, that is, a system, device, article, composition, formulation, or process that includes elements in addition to those listed after such a term in a claim are still deemed to fall within the scope of that claim. Moreover, in the following claims, the terms “first,” “second,” and “third,” etc. are used merely as labels, and are not intended to impose numerical requirements on their objects.
The above description is intended to be illustrative, and not restrictive. For example, the above-described examples (or one or more aspects thereof) may be used in combination with each other. Other embodiments can be used, such as by one of ordinary skill in the art upon reviewing the above description. The Abstract is provided to comply with 37 C.F.R. § 1.72(b), to allow the reader to quickly ascertain the nature of the technical disclosure. It is submitted with the understanding that it will not be used to interpret or limit the scope or meaning of the claims. Also, in the above Detailed Description, various features may be grouped together to streamline the disclosure. This should not be interpreted as intending that an unclaimed disclosed feature is essential to any claim. Rather, inventive subject matter may lie in less than all features of a particular disclosed embodiment. Thus, the following claims are hereby incorporated into the Detailed Description as examples or embodiments, with each claim standing on its own as a separate embodiment, and it is contemplated that such embodiments can be combined with each other in various combinations or permutations. The scope of the invention should be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.
This application claims the benefit of priority under 35 U.S.C. § 119(e) of Wagner et al., U.S. Provisional Patent Application Ser. No. 61/663,452, entitled “MODULAR ELBOW PROSTHESIS,” filed on Jun. 22, 2012, which is herein incorporated by reference in its entirety. This application is related to U.S. Ser. No. 13/800,567, filed on the same day as this application, entitled “ELBOW PROSTHESIS.”
Number | Name | Date | Kind |
---|---|---|---|
750678 | Morton | Jan 1904 | A |
1110528 | Borresen | Sep 1914 | A |
1517162 | King | Nov 1924 | A |
1677365 | Peck | Jul 1928 | A |
2462536 | Muter | Feb 1949 | A |
2737917 | Steele | Mar 1956 | A |
2837951 | Phelps | Jun 1958 | A |
3157075 | Filia | Nov 1964 | A |
3187751 | Coren | Jun 1965 | A |
3563124 | Gargrave | Feb 1971 | A |
3641652 | Arnold et al. | Feb 1972 | A |
3708805 | Scales et al. | Jan 1973 | A |
3816854 | Schlein | Jun 1974 | A |
3826160 | Allen et al. | Jul 1974 | A |
4038704 | Ring | Aug 1977 | A |
4227299 | Kuehling | Oct 1980 | A |
4280231 | Swanson | Jul 1981 | A |
4306550 | Forte | Dec 1981 | A |
4365411 | Muldoon | Dec 1982 | A |
4383337 | Volz et al. | May 1983 | A |
4420879 | Harringer | Dec 1983 | A |
4587964 | Walker et al. | May 1986 | A |
4765328 | Keller et al. | Aug 1988 | A |
4822364 | Inglis et al. | Apr 1989 | A |
4982631 | Lowther | Jan 1991 | A |
5020399 | Annis et al. | Jun 1991 | A |
RE33714 | Anderson | Oct 1991 | E |
5061271 | Van Zile | Oct 1991 | A |
5197368 | Meyer et al. | Mar 1993 | A |
5314479 | Rockwood, Jr. et al. | May 1994 | A |
5376121 | Huene et al. | Dec 1994 | A |
5702457 | Walch et al. | Dec 1997 | A |
5702486 | Craig et al. | Dec 1997 | A |
5723015 | Risung et al. | Mar 1998 | A |
5961555 | Hubner | Oct 1999 | A |
6027534 | Wack et al. | Feb 2000 | A |
6102953 | Huebner | May 2000 | A |
6129764 | Servidio | Oct 2000 | A |
6168630 | Keller et al. | Jan 2001 | B1 |
6197063 | Dews | Mar 2001 | B1 |
6290725 | Weiss et al. | Sep 2001 | B1 |
6314843 | Wiebe et al. | Nov 2001 | B1 |
6379387 | Tornier | Apr 2002 | B1 |
6673114 | Hartdegen et al. | Jan 2004 | B2 |
6699290 | Wack et al. | Mar 2004 | B1 |
6716218 | Holmes | Apr 2004 | B2 |
6716248 | Huene | Apr 2004 | B2 |
6739068 | Rinner | May 2004 | B1 |
6767368 | Tornier | Jul 2004 | B2 |
6890357 | Tornier | May 2005 | B2 |
6923832 | Sharkey et al. | Aug 2005 | B1 |
6964088 | Crevoisier | Nov 2005 | B2 |
6969407 | Klotz et al. | Nov 2005 | B2 |
7097663 | Nicol et al. | Aug 2006 | B1 |
7247170 | Graham et al. | Jul 2007 | B2 |
7338528 | Stone et al. | Mar 2008 | B2 |
7604666 | Berelsman et al. | Oct 2009 | B2 |
7625406 | Berelsman et al. | Dec 2009 | B2 |
7722625 | Sanders et al. | May 2010 | B2 |
7846376 | Abt et al. | Dec 2010 | B2 |
7850737 | Morrey | Dec 2010 | B2 |
8328873 | Metzger et al. | Dec 2012 | B2 |
8753348 | DiDomenico | Jun 2014 | B2 |
8936647 | Wagner et al. | Jan 2015 | B2 |
8968411 | Wagner et al. | Mar 2015 | B2 |
20010021876 | Terril-Grisoni et al. | Sep 2001 | A1 |
20020156534 | Grusin et al. | Oct 2002 | A1 |
20020165614 | Tornier | Nov 2002 | A1 |
20030144739 | Huene | Jul 2003 | A1 |
20030208276 | Berelsman et al. | Nov 2003 | A1 |
20030208277 | Weiss et al. | Nov 2003 | A1 |
20040186581 | Huene | Sep 2004 | A1 |
20040193268 | Hazebrouck | Sep 2004 | A1 |
20040193276 | Maroney et al. | Sep 2004 | A1 |
20040243243 | Tornier | Dec 2004 | A1 |
20050043806 | Cook et al. | Feb 2005 | A1 |
20050075735 | Berelsman et al. | Apr 2005 | A1 |
20060100712 | Ball | May 2006 | A1 |
20060100713 | Ball | May 2006 | A1 |
20060111788 | Ball | May 2006 | A1 |
20060111789 | Ball | May 2006 | A1 |
20060173546 | Berelsman et al. | Aug 2006 | A1 |
20060224243 | Pare et al. | Oct 2006 | A1 |
20060247786 | Ball | Nov 2006 | A1 |
20070129808 | Justin et al. | Jun 2007 | A1 |
20070282450 | Habermeyer et al. | Dec 2007 | A1 |
20070299527 | Mccleary et al. | Dec 2007 | A1 |
20080015706 | Berelsman et al. | Jan 2008 | A1 |
20080033566 | Berelsman et al. | Feb 2008 | A1 |
20080114461 | Collazo | May 2008 | A1 |
20080306601 | Dreyfuss | Dec 2008 | A1 |
20090024221 | Ball | Jan 2009 | A1 |
20090105839 | Ikegami et al. | Apr 2009 | A1 |
20090312840 | Morrey | Dec 2009 | A1 |
20100051141 | Bhambri | Mar 2010 | A1 |
20100087928 | Graham et al. | Apr 2010 | A1 |
20100160985 | Pannu | Jun 2010 | A1 |
20100179661 | Berelsman et al. | Jul 2010 | A1 |
20100222887 | Katrana et al. | Sep 2010 | A1 |
20110125274 | Bartel et al. | May 2011 | A1 |
20110153024 | Wagner et al. | Jun 2011 | A1 |
20110172781 | Katrana et al. | Jul 2011 | A1 |
20120000326 | Sheriff | Jan 2012 | A1 |
20120095473 | Soliman | Apr 2012 | A1 |
20130345818 | Wagner et al. | Dec 2013 | A1 |
20140012338 | Kirschman | Jan 2014 | A1 |
20140165793 | Legg | Jun 2014 | A1 |
20150088263 | Wagner et al. | Mar 2015 | A1 |
Number | Date | Country |
---|---|---|
104602648 | May 2015 | CN |
7144144 | Mar 1972 | DE |
2863845 | Apr 2015 | EP |
2575384 | Jul 1986 | FR |
2579454 | Oct 1986 | FR |
2660857 | Dec 1997 | FR |
WO-8904238 | May 1989 | WO |
WO-9725943 | Jul 1997 | WO |
WO-2006129495 | Dec 2006 | WO |
WO-2008002545 | Jan 2008 | WO |
WO-2010098791 | Sep 2010 | WO |
WO-2011060430 | May 2011 | WO |
WO-2013192408 | Dec 2013 | WO |
Entry |
---|
“U.S. Appl. No. 12/856,112, Non Final Office Action dated Mar. 14, 2014”, 10 pgs. |
“U.S. Appl. No. 12/856,112, Notice of Allowance dated Oct. 24, 2014”, 8 pgs. |
“U.S. Appl. No. 12/856,112, Response filed Jun. 16, 2014 to Non-Final Office Action dated Mar. 14, 2014”, 11 pgs. |
“U.S. Appl. No. 13/800,567, Non Final Office Action dated Jan. 29, 2014”, 14 pgs. |
“U.S. Appl. No. 13/800,567, Notice of Allowance dated Sep. 3, 2014”, 10 pgs. |
“U.S. Appl. No. 13/800,567, Response filed May 29, 2014 to Non Final Office Action dated Jan. 29, 2014”, 19 pgs. |
“U.S. Appl. No. 14/559,121, Prleliminary Amendment filed Dec. 4, 2014”, 7 pgs. |
“International Application Serial No. PCT/US2013/046792, International Preliminary Report on Patentability dated Dec. 31, 2014”, 9 pgs. |
“U.S. Appl. No. 14/559,121, Non Final Office Action dated Feb. 11, 2016”, 7 pgs. |
“U.S. Appl. No. 14/559,121, Notice of Allowance dated Jun. 28, 2016”, 5 pgs. |
“U.S. Appl. No. 14/559,121, Response filed May 11, 2016 to Non Final Office Action dated Feb. 11, 2016”, 8 pgs. |
“U.S. Appl. No. 14/559,121, Response filed Nov. 2, 2015 to Restriction Requirement dated Sep. 2, 2015”, 11 pgs. |
“U.S. Appl. No. 14/559,121, Restriction Requirement dated Sep. 2, 2015”, 7 pgs. |
“Chinese Application Serial No. 201380042656.3, Office Action dated Oct. 8, 2015”, (W/ English Translation), 16 pgs. |
“Chinese Application Serial No. 201380042656.3, Response filed Mar. 23, 2016 to Office Action dated Oct. 8, 2015”, (W English Translation), 16 pgs. |
“U.S. Appl. No. 15/278,982, Final Office Action dated Jan. 26, 2018”, 16 pgs. |
“U.S. Appl. No. 15/278,982, Response filed Dec. 5, 2017 to Non Final Office Action dated Sep. 5, 2017”, 13 pgs. |
“U.S. Appl. No. 12/856,112, Advisory Action dated Aug. 15, 2013”, 3 pgs. |
“U.S. Appl. No. 12/856,112, Response filed Aug. 23, 2013 to Final Office Action dated Apr. 26, 2013 and Advisory Action dated Aug. 15, 2013”, 12 pgs. |
“U.S. Appl. No. 13/800,567, Response filed Oct. 9, 2013 to Restriction Requirement dated Sep. 10, 2013”, 10 pgs. |
“U.S. Appl. No. 13/800,567, Restriction Requirement dated Sep. 10, 2013”, 7 pgs. |
“International Application Serial No. PCT/US2013/046792, International Search Report dated Aug. 23, 2013”, 6 pgs. |
“International Application Serial No. PCT/US2013/046792, Written Opinion dated Aug. 23, 2013”, 7 pgs. |
“U.S. Appl. No. 12/856,112, Examiner Interview Summary dated Jul. 11, 2013”, 3 pgs. |
“U.S. Appl. No. 12/856,112, Examiner Interview Summary dated Dec. 17, 2012”, 5 pgs. |
“U.S. Appl. No. 12/856,112, Final Office Action dated Apr. 26, 2013”, 9 pgs. |
“U.S. Appl. No. 12/856,112, Non Final Office Action dated May 30, 2012”, 11 pgs. |
“U.S. Appl. No. 12/856,112, Response filed May 14, 2012 to Restriction Requirement dated Apr. 13, 2012”, 9 pgs. |
“U.S. Appl. No. 12/856,112, Response filed Jul. 1, 2013 to Final Office Action dated Apr. 26, 2013”, 12 pgs. |
“U.S. Appl. No. 12/856,112, Response filed Nov. 30, 2012 to Non Final Office Action dated May 30, 2012”, 18 pgs. |
“U.S. Appl. No. 12/856,112, Restriction Requirement dated Apr. 13, 2012”, 7 pgs. |
“The Ball Lock System—Dayton True Position Retainers”, Brochure; Dayton Progress Corporation, (2002), 6 pgs. |
“Zimmer Coonrad/Morrey Total Elbow Arthroplastly—Impaction Grafting Procedure”, Surgical Technique for Revision; Zimmer, Inc., (2002), 2 pgs. |
“Zimmer Coonrad/Morrey Total Elbow, Interchangeability, Anterior Flange, Clinical History”, Surgical Technique; 97-8106-102-00 Rev. 2, Zimmer, Inc., (2002, 2005, 2009), 11 pgs. |
“Zimmer Coonrad/Morrey Total Elbow, Interchangeability, Anterior Flange, Clinical Success”, Brochure; 97-8106-301-00 Zimmer, Inc., (2000, 2006, 2007), 4 pgs. |
Number | Date | Country | |
---|---|---|---|
20130340236 A1 | Dec 2013 | US |
Number | Date | Country | |
---|---|---|---|
61663452 | Jun 2012 | US |