System for fracture replacement of comminuted bone fractures or portions thereof adjacent bone joints

Information

  • Patent Grant
  • 11266506
  • Patent Number
    11,266,506
  • Date Filed
    Monday, December 23, 2019
    4 years ago
  • Date Issued
    Tuesday, March 8, 2022
    2 years ago
Abstract
The system and method serves in facilitating replacement of comminuted bone fractures or portions thereof adjacent bone joints. The system and method employs a prosthesis to replace at least a portion of the comminuted bone fractures. The prosthesis serves in reproducing the articular surface of the portion or portions of the comminuted bone fractures that are replaced. In doing so, the prosthesis serves in restoring joint viability and corresponding articulation thereof.
Description
BACKGROUND
Field of the Invention

The present invention is generally related to a medical device and method for use thereof for facilitating replacement of comminuted bone fractures. In particular, the present invention is related to a system and method for use thereof to aid in the replacement of comminuted bone fractures adjacent bone joints to restore joint viability. More specifically, the present invention relates to a system and method for use thereof for replacing comminuted bone fractures adjacent joints by providing a prosthesis to replace the fractured bone to facilitate restoration of movement associated with the bone joint.


Description of the Prior Art

Comminuted bone fractures adjacent joints oftentimes result in significant fragmentation of the bone. In fact, these types of bone fractures can often result in portions of the bone being severely fragmented. That is, the number of fragments created by these types of bone factures pose difficulties in repairing the bone. Bone plates have oftentimes been used to aid repair of the comminuted bone fractures. However, even with use of bone plates, the comminuted bone fractures may not be adequately reconstructed. For example, if severely fragmented, the proximal and distal end portions of a humerus may not be reconstructible. As such, there is a need for a prosthesis affording replacement of the comminuted bone fractures or portions thereof to restore joint viability. The prosthesis can be used when the comminuted bone fractures need substantial support to aid repair or are irretrievably fragmented. Such a prosthesis, for example, can be configured to repair the proximal and distal ends of the humerus.


SUMMARY OF THE INVENTION

The present invention in one embodiment contemplates a method for replacing at least a portion of a comminuted humeral head, the method including the following acts. A prosthesis is provided that has an exterior portion having an exterior surface, and an interior portion having at least one aperture formed therein, the exterior surface approximating the surface of the at least a portion of the comminuted humeral head in size and shape, and the at least one aperture of the prosthesis being configured to receive at least one fastener therein. A bone plate is provided that has at least one opening formed therein, the at least one aperture of the bone plate being configured to receive the at least one fastener therethrough. At least a portion of the comminuted humeral head is removed. The bone plate is attached to at least a portion of a humerus. The at least one aperture of the prosthesis is aligned with the at least one opening of the bone plate. The at least one fastener is inserted through the at least one opening and into the at least one aperture. The prosthesis and the bone plate are securely attached to one another across the humerus using the fastener.


In another preferred embodiment, the present invention contemplates a system for replacement of at least a portion of a comminuted humeral head. The system includes a prosthesis, a bone plate, and at least one fastener. The prosthesis has an exterior portion having an exterior surface and an interior portion having at least one aperture formed therein, the exterior surface being sized and shaped to approximate the surface of the at least a portion of the comminuted humeral head, and the at least one aperture of the prosthesis configured to receive at least one fastener therein. The bone plate including at least one opening formed therein, the at least one opening of the bone plate being configured to receive the at least one fastener therethrough. The at least one fastener having a first end for insertion through the at least one opening and into the at least one aperture, the at least one fastener being configured to secure attachment of the prosthesis and the bone plate to one another across a portion of a humerus.


In yet another preferred embodiment, the present invention contemplates a method for replacing at least a portion of a fractured capitellum and/or a fractured trochlea, the method including the following acts. An apparatus is provided that has a prosthesis portion and a plate portion, the prosthesis portion having an exterior surface, and the plate portion including a first leg portion extending outwardly from the prosthesis portion and a second leg portion extending outwardly from the prosthesis portion. At least a portion of the fractured capitellum and/or the fractured trochlea is removed. The prosthesis portion is sized and shaped according to the portion of the fractured capitellum and/or the fractured trochlea removed, the prosthesis portion having an exterior surface approximating the exterior surface of the removed portion of the fractured capitellum and/or the fractured trochlea. The prosthesis portion is positioned relative to the humerus. The first leg portion is attached to the lateral column of the humerus and the second leg portion is attached to the medial column of the humerus.


It is understood that both the foregoing general description and the following detailed description are exemplary and exemplary only, and are not restrictive of the invention as claimed.





BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are incorporated in and constitute a part of the specification, illustrate preferred embodiments of the invention. Together with the description, they serve to explain the objects, advantages and principles of the invention. In the drawings:



FIG. 1 is a perspective view of a first embodiment of a system for fracture repair and/or replacement for use with and depicted as attached to a proximal portion of a humerus;



FIG. 2 is the perspective view of FIG. 1 showing a humeral head prosthesis, an extension portion, and fasteners of the first embodiment of the system in phantom with respect to the humerus;



FIG. 3 is a perspective view of a second embodiment of the system for fracture repair and/or replacement for use with a distal portion of the humerus;



FIG. 4 is a front elevational view of the second embodiment of the system depicted in FIG. 3;



FIG. 5 is a side elevational view of the second embodiment of the system depicted in FIGS. 3 and 4;



FIG. 6 is a cross-sectional view of the second embodiment of the system depicted in FIGS. 3-5 taken along Line 6-6 of FIG. 4; and



FIG. 6A is a alternative cross section for the second embodiment of the system depicted in FIGS. 3-6.





DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The systems for fracture replacement of comminuted bone fractures or portions thereof and the method for use of the system are depicted in the accompanying drawings. The systems of the present invention provide a prosthesis affording replacement of the comminuted bone fractures or portions thereof. While the below-described systems are used in association with the proximal and distal end portions of a humerus, the present invention is not limited thereto. That is, the system and method of the present invention can be configured for use elsewhere in the human body.


A first illustrative embodiment of the system is generally indicated by the numeral 10 in FIGS. 1 and 2, and a second illustrative embodiment of the system is generally indicated by the numeral 100 in FIGS. 3-6A. First system 10 is used in replacing a fractured humeral head or portions thereof at the proximal end of the humerus and second system 100 is used in replacing a fractured capitellum and/or a fractured trochlea or portions thereof at the distal end of the humerus. In doing so, first and second systems 10 and 100 serve to repair the proximal and distal ends, respectively, of the humerus, and serve in restoring joint viability. The components of each of systems 10 and 100 are constructed of metal or other artificial material suitable for human implantation.


First system 10 is provided to facilitate replacement of a humeral head or portions thereof (not shown) at the proximal end of a humerus H (FIGS. 1 and 2) that have been irretrievably fragmented. Furthermore, while first system 10 is depicted replacing the humeral head or portion thereof, first system 10, for example, could be configured for replacing portions of a distal ulna. First system 10 includes a head portion 12 (or prosthetic portion), an optional extension portion 14 (of the medial calcar), and a bone plate 16. Head portion 12 serves as prosthesis for replacement of the humeral head or portions thereof, and bone plate 16 is configured to provided a rigid structure for attaching head portion 12 and extension portion 14 thereto. Extension portion 14 provides additional structural integrity, but, depending on the needs of the patient, may not be necessary.


Bone plate 16 is attached to surgical neck SN of humerus H. Bone plate 16 is configured to receive one or more bone screws 18 therethrough for attachment to surgical neck SN. Bone screws 18 are exclusively used for attachment of bone plate 16 to surgical neck SN.


Bone plate 16 also is configured to receive fasteners (such as bolts, posts, and/or screws) 20 and 22 for engagement with head portion 12 and extension portion 14, respectively. If fasteners 20 and 22 are bolts and/or screws, then fasteners 20 and 22 could threadably engage head portion 12 and extension portion 14, respectively, to facilitate attachment. Furthermore, if fasteners 20 and 22 are posts, then fasteners 20 and 22 could be attached to head portion 12 and extension portion 14, respectively, using interference fits therebetween. Thus, whether fasteners 20 and 22 are bolts, posts, and/or screws, the fasteners, and head portion 12 and extension portion 14 would include complementary structures facilitating attachment.


To facilitate engagement of bone plate 16 with head portion 12 and extension portion 14 using fasteners 20 and 22, respectively, bone plate 16 includes openings 24 and 26 therethrough. Openings 24 are provided at or adjacent the upper portion of bone plate 16 for receiving fasteners 20, and openings 26 are provided at or adjacent the middle portion of bone plate 16 for receiving fasteners 22. After insertion thereof through bone plate 16, fasteners 20 and 22 engage head portion 12 and extension portion 14, respectively, to provide for the rigid attachment of humeral head prosthesis 10 to humerus H. In addition to threads (not shown) or structures (not shown) for providing for an interference fit to facilitate engagement with head portion 12 and extension portion 14, fasteners 20 and 22 can include threads (not shown) for engaging complementary threads (not shown) provided in openings 24 and 26 to lock fasteners 20 and 22 to bone plate 16. Moreover, fasteners 20 and 22 could include threads facilitating attachment to portions of humerus H that fasteners 20 and 22 extend through.


Head portion 12 can be sized and shaped according to the portions of the humeral head being replaced. As such, portions of head portion 12 serve in reproducing the articular surface of the proximal humerus that is being replaced using system 10. Thus, if only a portion of the humeral head requires replacement, head portion 12 can be sized and shaped to approximate the size and shape of the portion of the humeral head being replaced. However, if the entirety of the humeral head is being replaced, head portion 12 can be sized and shaped to approximate the size and shape of the entirety of the humeral head. As depicted in FIGS. 1 and 2, head portion 12 is sized and shaped to replace the entirety of the humeral head.


Head portion 12 includes an exterior-facing portion having an exterior surface 30, and an interior-facing portion of having an interior surface 32, columns 34, and apertures 36 for receiving fasteners 20 therein. Apertures 36 can include complementary threads (not shown) or structures (not shown) for providing an interference fit to facilitate engagement with fasteners 20. As depicted in FIGS. 1 and 2, exterior surface 30 is convex and is configured to mimic the shape of the humeral head or portions thereof to reproduce the articular surface of the proximal humerus being replaced. Accordingly, portions of exterior surface 30 can be highly polished or lubricated. Furthermore, as depicted in FIG. 2, interior surface 32 is concave, and columns 34 extend outwardly from interior surface 32.


Columns 34 include apertures 36 for receiving fasteners 20 therein. However, the present invention is not limited to using columns 34. For example, if interior surface 32 is flattened (rather than concave) and an adequate depth of material is provided between exterior surface 30 and interior surface 32, apertures 36 could be formed through interior surface 32 into the material provided between exterior surface 30 and interior surface 32.


Furthermore, relief holes 38 are provided through columns 34 to communicate with apertures 36. Relief holes 38 allow tissues, fluids, and/or air that were present in apertures 36 (prior to insertion of fasteners 20 therein) to be expelled therefrom as fasteners 20 are tightened in position.


While head portion 12 is depicted in FIGS. 1 and 2 as being a single integral component, head portion 12 can be composed of two or more elements that can be integrated with one another during implantation of system 10. For example, head portion 12 could be composed of a base plate (not shown) and a portion (not shown) including exterior surface 30. The base plate would first be attached to bone plate 16 using fasteners 20, and then the portion including exterior surface 30 would be attached to the base plate. The base plate and the portion including exterior surface 30 could include a complementary attachment mechanism shared therebetween to facilitate integration thereof. As such, a standard sized and shaped base plate could be utilized, and only the portion including exterior surface 30 would be sized and shaped according to the portions of the humeral head being replaced.


Extension portion 14, as depicted in FIG. 2, depends downwardly from head portion 12. Extension portion 14 is inserted into medullary cavity MC, and is configured to interface with the bone adjacent medullary cavity MC. Furthermore, using fasteners 22, extension portion 14 can be attached to the medial cortex of humerus H. To that end, extension portion 14 includes apertures 40 for receiving fasteners 22. Like apertures 36 of head portion 12, apertures 40 can also include complementary threads (not shown) or structures (not shown) for providing an interference fit to facilitate engagement with fasteners 22.


Rather than or in addition to using fasteners 20 and 22, integral posts (not shown) formed with bone plate 16 could be used to attach bone plate 16 with head portion 12 and/or extension portion 14. For example, an integral post that extends outwardly from bone plate 16 could be positioned adjacent apertures 24. Furthermore, a portion of the integral post could be received in one of apertures 36, and the integral post and the one of apertures 36 could include complementary structures (not shown) facilitating attachment therebetween.


Moreover, while fasteners 20 and 22 are shown as being inserted through bone plate 16 and into head portion 12 and extension portion 14, respectively, head portion 12, extension portion 14, and bone plate 16 could be configured to provide the opposite arrangement—fasteners 20 and 22 could be inserted through head portion 12 and extension portion 14, respectively, and into bone plate 16. As such, head portion 12, extension portion 14, and bone plate 16 would include complementary configurations to afford such an arrangement. For example, head portion 12 could include an opening (not shown) extending through the exterior-facing portion and the interior-facing portion thereof. Thus, a fastener (similar, if not identical, to fastener 20) could be inserted through such an opening and into a corresponding aperture formed in bone plate 16.


To secure attachment of first system 10 to humerus H using the configuration thereof depicted in FIGS. 1 and 2, the fractured humeral head or portions thereof are removed from adjacent humerus H. Bone plate 16 is initially attached to surgical neck SN using bone screw 18. Thereafter, openings 24 and 26 through bone plate 16 can be used as drill guides for receiving a drill to create alignment holes through humerus H. The alignment holes created by the drill will ultimately afford alignment between holes 24 in bone plate 16 and apertures 36 in head portion 12, and between holes 26 in bone plate 16 and apertures 40 in extension portion 14. Once the alignment holes are created, head portion 12 is positioned with respect to humerus H. Fasteners 20 and 22 are then inserted through openings 24 and 26 into apertures 36 and 49, respectively. Tightening of fasteners 20 and 22 in holes 36 and 40 serve to secure engagement of head portion 12 to humerus 10. As such, head portion 12, extension portion 14, and bone plate 16 and fasteners 20 and 22 extending therebetween provide an effective structural lattice allowing head portion 12 to provide an effective replacement for the humeral head or portions thereof that are severely fractured. Via replacement of the humeral head or portions thereof using first system 10, the viability of the shoulder joint adjacent to head portion 12 can be restored.


As discussed above, second system 100 is provided to facilitate replacement of a fractured capitellum and/or a fractured trochlea or portions thereof (not shown) at the distal end of the humerus. As depicted in FIGS. 3-6A, second system 100 includes a prosthetic portion 102 and a plate portion 104. Prosthetic portion 102 and plate portion 104 are depicted in FIGS. 3-6A as being formed integrally with one another. However, second system 100 is not limited thereto. Prosthetic portion 102 and plate portion 104 can be formed separately from one another and then cooperatively engaged to (or integrated with) one another. For example, prosthetic portion 102 and plate portion 104 could be fastened to one another using a fastener extending through portions thereof during implantation of system 100. Furthermore, while second system 100 is configured to replace the fractured capitellum and/or the fractured trochlea or portions thereof, second system 100 is not limited thereto. For example, second system 100 also could be configured to replace fractured portions of the humerus such as the lateral epicondyle, the olecranon fossa, and/or medial epicondyle.


Prosthetic portion 102 serves as a prosthesis for replacement of the fractured capitellum and/or the fractured trochlea or portions thereof. As such, prosthetic portion 102 could be shaped to replace the entirety of both of the fractured capitellum and the fractured trochlea, or various portions of the fractured capitellum and/or the fractured trochlea. Furthermore, plate portion 104 is configured to provide a rigid structure for attaching prosthetic portion 102 to the humerus.


As depicted in FIGS. 3-5, prosthetic portion 102 includes a capitellum portion 106 and a trochlea portion 108. As discussed above, the entirety of the fractured capitellum and/or the fractured trochlea or portions thereof can be replaced using prosthetic portion 102. Thus, prosthetic portion 102 includes an exterior surface 110 (extending over capitellum portion 106 and trochlea portion 108) that can be sized and shaped according to the portions of the fractured capitellum and/or the fractured trochlea requiring replacement. As such, portions of prosthetic portion 102 serve in reproducing the articular surface of the distal humerus that is being replaced using system 100. Accordingly, portions of exterior surface 110 can be highly polished or lubricated.


For example, if only the entirety of fractured capitellum requires replacement, then prosthetic portion 102 (and exterior surface 110 thereof) would be sized and shaped to approximate the entirety of the capitellum and could incorporate only capitellum portion 106. Furthermore, if only the entirety of the fractured trochlea requires replacement, prosthetic portion 102 (and exterior surface 110 thereof) would be sized and shaped to approximate the entirety of the trochlea and could incorporate only trochlea portion 108. However, if only selected portions of the fractured capitellum and the fractured trochlea require replacement, then prosthetic portion 102 (and exterior surface 110 thereof) would be sized and shaped to approximate the selected portions by incorporating corresponding portions of capitellum portion 106 and trochlea portion 108.


Furthermore, prosthetic portion 102 can be constructed to be hollow to include a cavity 112. As depicted in FIGS. 3 and 6, cavity 112 is formed behind exterior surface 110, and thus, an interior surface 114 (of cavity 112) is opposite exterior surface 110. Cavity 112 can be filled with bone graft materials, and/or portions of the fractured capitellum and the fractured trochlea that the prosthetic portion 102 is being used to replace. Alternatively, prosthetic portion 102 can be constructed of solid material as depicted in the cross-sectional view of FIG. 6A. As such, prosthetic portion 102 would be formed of solid material approximating the portions of the fractured capitellum and/or the fractured trochlea being replaced.


As depicted in FIGS. 3 and 4, plate portion 104 extends outwardly from prosthetic portion 102, and includes a body portion 120, a first leg portion 122, and a second leg portion 124. First leg portion 122 extends outwardly from capitellum portion 106, and second leg portion 124 extends outwardly from trochlea portion 108. Furthermore, first and second leg portions 122 and 124 extend from prosthetic portion 102 to terminate at body portion 120.


An aperture 130, as depicted in FIGS. 3 and 4 is formed between prosthesis portion 102 and first and second leg portions 122 and 124. Furthermore, plate portion 104 includes a front surface 132 and a rear surface 134 opposite the front surface 132. As discussed below, portions of rear surface 134 (which encompasses body portion 120, first leg portion 122, and second leg portion 124) is engaged to portions of the humerus. As such, rear surface 134 can be at least in part concave (FIG. 6) to facilitate such engagement.


Body portion 120 is attached to the shaft (not shown) of the humerus. Furthermore, first leg portion and second leg portions 122 and 124 are attached to the humerus—first leg portion 120 is attached to the lateral column (not shown) and second leg portion 122 is attached to the medial column (not shown). To that end, body portion 120, first leg portion 122, and second leg portion 124 can include various apertures 126. Apertures 126 can be configured to receive bone screws (not shown) therethrough to attach plate portion 104 to the humerus.


In addition to threads (not shown) for engaging the humerus, the bone screws used to attach the plate portion thereto can include threads (not shown) for engaging complementary threads (not shown) provided in apertures 126 to lock the bone screws to plate portion 104. Furthermore, if necessary, a second plate portion (not shown) can be positioned on the opposite side of the humerus of plate portion 104 to afford another attachment structure for plate portion 104. Thus, additional fasteners (such as bolts and/or screws) could be used to interconnect plate portion 104 and the second plate portion to further enhance the rigidity of the structure attaching prosthetic portion 102 to the humerus.


To secure attachment of the first system 100 to the humerus, the fractured capitellum and/or the fractured trochlea or portions thereof are removed from adjacent the humerus. Thereafter, plate portion 104 is attached to the humerus with or without drilling into the humerus. If holes are drilled in the humerus to receive the bone screws, apertures 126 through plate portion 104 can be used as drill guides for receiving a drill. The bone screws are thereafter inserted through apertures 126 and into the humerus. Using the bone screws to facilitate attachment to the humerus, body portion 120 is attached to the shaft, first leg portion 120 is attached to the lateral column, and second leg portion 122 is attached to the medial column. The attachment of body portion 120, first leg portion 122, and second leg portion 124 to the humerus provides the structural rigidity necessary to allow prosthetic portion 102 to provide an effective replacement for the fractured capitellum and/or the fractured trochlea or portions thereof. Via replacement of the fractured capitellum and/or the fractured trochlea or portions thereof using second system 100, the viability of the elbow joint adjacent to prosthesis portion 102 can be restored.


In summary, systems 10 and 100 for replacement of comminuted bone portions and the method for use thereof provide a prosthesis affording replacement of the comminuted bone fractures or portions thereof. Furthermore, while systems 10 and 100 are used in association with the proximal and distal end portions, respectively, of the humerus, the system and method of the present invention can be configured for use elsewhere in the human body. Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. Accordingly, it is intended that the specification and examples be considered as exemplary only.

Claims
  • 1. A system for replacement of at least a portion of a fractured capitellum and/or a fractured trochlea of a humerus of an elbow joint, the system comprising: a prosthesis portion having an exterior surface sized and shaped to reproduce a removed portion of the fractured capitellum and/or the fractured trochlea, and the exterior surface of the prosthesis portion is configured to replicate at least a portion of the articular surface of the elbow joint; anda plate portion including a first leg portion extending outwardly from the prosthesis portion and a second leg portion extending outwardly from the prosthesis portion, the first leg portion including a first contact surface configured to contact a lateral column of the humerus, and the second leg portion including a second contact surface configured to contact a medial column of the humerus;wherein the first leg portion is attachable to the lateral column of the humerus and the second leg portion is attachable to the medial column of the humerus, and the exterior portion of the prosthesis portion is usable to form a portion of the elbow joint.
  • 2. The system of claim 1, wherein the plate portion includes a body portion, the body portion connecting portions of the first leg portion and the second leg portion to one another, and being attachable to the humerus.
  • 3. The system of claim 2, wherein the first leg portion and the second portion are spaced apart from one another between the prosthesis portion and the body portion.
  • 4. The system of claim 2, wherein each of the first leg portion, the second leg portion, and the body portion include apertures for facilitating attachment of the plate portion to bone.
  • 5. The system of claim 2, wherein the body portion includes a third contact surface, at least portions of the first contact surface, the second contact surface, and the third contact surface being concave.
  • 6. The system of claim 1, wherein the prosthesis portion includes an interior surface opposite the exterior surface, the interior surface forming a cavity, and the cavity being adapted to receive bone graft materials.
  • 7. The system of claim 1, wherein the prosthesis portion reproduces the removed portions of both of the fractured capitellum and the fractured trochlea.
  • 8. A system for replacement of at least a portion of a fractured capitellum and/or a fractured trochlea of a humerus of an elbow joint, the system comprising: a prosthesis portion having an exterior surface sized and shaped to reproduce an articular surface of a removed portion of the fractured capitellum and/or the fractured trochlea; anda plate portion extending outwardly from the prosthesis portion, the plate portion including a contact surface configured to contact at least one of a lateral column and a medial column of the humerus;wherein the plate portion is attachable to the at least one of the lateral column and the medial column of the humerus, and the exterior portion of the prosthesis portion is usable to form a portion of the elbow joint.
  • 9. The system of claim 8, wherein the plate portion includes a body portion, a first leg portion, and a second leg portion, the body portion connecting portions of the first leg portion and the second leg portion to one another.
  • 10. The system of claim 9, wherein the first leg portion and the second portion are spaced apart from one another between the prosthesis portion and the body portion.
  • 11. The system of claim 9, wherein each of the first leg portion, the second leg portion, and the body portion include apertures for facilitating attachment of the plate portion to bone.
  • 12. The system of claim 9, wherein the contact surface of the plate portion extends along one of the first leg portion and the second leg portion, and at least a portion of the contact surface is concave.
  • 13. The system of claim 8, wherein the prosthesis portion includes an interior surface opposite the exterior surface, the interior surface forming a cavity, and the cavity being adapted to receive bone graft materials.
  • 14. The system of claim 8, wherein the prosthesis portion reproduces the removed portions of both of the fractured capitellum and the fractured trochlea.
  • 15. A system for replacement of at least portions of a fractured capitellum and a fractured trochlea of a humerus of an elbow joint, the system comprising: a prosthesis portion having an exterior surface sized and shaped to reproduce removed portions of the fractured capitellum and the fractured trochlea, and the exterior surface of the prosthesis portion is configured to replicate portions of the articular surface of the elbow joint; anda plate portion extending outwardly from the prosthesis portion, the plate portion including a contact surface configured to contact at least one of a lateral column and a medial column of the humerus;wherein the plate portion is attachable to the at least one of the lateral column and the medial column of the humerus.
  • 16. The system of claim 15, wherein the plate portion includes a body portion, a first leg portion, and a second leg portion, the body portion connecting portions of the first leg portion and the second leg portion to one another.
  • 17. The system of claim 16, wherein the first leg portion and the second portion are spaced apart from one another between the prosthesis portion and the body portion.
  • 18. The system of claim 16, wherein each of the first leg portion, the second leg portion, and the body portion include apertures for facilitating attachment of the plate portion to bone.
  • 19. The system of claim 15, wherein the prosthesis portion includes an interior surface opposite the exterior surface, the interior surface forming a cavity, and the cavity being adapted to receive bone graft materials.
  • 20. The system of claim 15, wherein the prosthesis portion reproduces the removed portions of both of the fractured capitellum and the fractured trochlea.
RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 15/702,006, filed Sep. 12, 2017 (U.S. Pat. No. 10,524,919); which is a divisional of U.S. application Ser. No. 14/522,702, filed Oct. 24, 2014 (U.S. Pat. No. 9,757,240); which is a divisional of U.S. application Ser. No. 13/282,810, filed Oct. 27, 2011 (U.S. Pat. No. 8,870,963); which claims the benefit of U.S. Provisional Application No. 61/407,072, filed Oct. 27, 2010, entitled “Proximal Humerus Hybrid Prosthesis Plate and Method of Use Associated Therewith”; all of which are incorporated by reference herein.

US Referenced Citations (262)
Number Name Date Kind
1950799 Jones Mar 1934 A
2500370 McKibbin Mar 1950 A
2555291 Poupitch May 1951 A
2580821 Toufick Jan 1952 A
2682265 Collison Jun 1954 A
2853114 Barry Sep 1958 A
2875663 Wieber Mar 1959 A
3489143 Halloran Jan 1970 A
3552389 Allgower et al. Jan 1971 A
3579831 Stevens et al. May 1971 A
3716050 Johnston Feb 1973 A
3791380 Dawidowski Feb 1974 A
3824995 Getscher Jul 1974 A
3900025 Barnes, Jr. Aug 1975 A
4029091 von Bezold Jun 1977 A
4263904 Judet Apr 1981 A
4535768 Hourahane et al. Aug 1985 A
4683878 Carter Aug 1987 A
4733654 Marino Mar 1988 A
4776330 Chapman et al. Oct 1988 A
4790302 Colwill et al. Dec 1988 A
4794919 Nilsson Jan 1989 A
4796612 Reese Jan 1989 A
4838264 Bremer et al. Jun 1989 A
4858602 Seidel et al. Aug 1989 A
4870957 Goble et al. Oct 1989 A
5003969 Azer et al. Apr 1991 A
5015248 Burstein et al. May 1991 A
5041113 Biedermann et al. Aug 1991 A
5041114 Chapman et al. Aug 1991 A
5180383 Haydon Jan 1993 A
5190544 Chapman et al. Mar 1993 A
5324291 Ries et al. Jun 1994 A
5356410 Pennig Oct 1994 A
5364399 Lowery et al. Nov 1994 A
5423860 Lizardi et al. Jun 1995 A
5437667 Papierski et al. Aug 1995 A
5443516 Albrektsson et al. Aug 1995 A
5458654 Tepic Oct 1995 A
5462547 Weigum Oct 1995 A
5472444 Huebner et al. Dec 1995 A
5505734 Caniggia et al. Apr 1996 A
5578035 Lin Nov 1996 A
5584835 Greenfield Dec 1996 A
5586985 Putnam et al. Dec 1996 A
5601553 Trebing et al. Feb 1997 A
5620449 Faccioli et al. Apr 1997 A
5658287 Hofmann et al. Aug 1997 A
5665088 Gil et al. Sep 1997 A
5674222 Berger et al. Oct 1997 A
5676667 Hausman Oct 1997 A
5681311 Foley et al. Oct 1997 A
5709686 Talos et al. Jan 1998 A
5725593 Caracciolo Mar 1998 A
5749872 Kyle et al. May 1998 A
5766174 Perry Jun 1998 A
5776194 Mikol et al. Jul 1998 A
5779704 Kim Jul 1998 A
5785712 Runciman et al. Jul 1998 A
5840078 Yerys Nov 1998 A
5868749 Reed Feb 1999 A
5931839 Medoff Aug 1999 A
5976139 Bramlet Nov 1999 A
5980575 Albrektsson et al. Nov 1999 A
6030389 Wagner et al. Feb 2000 A
6096040 Esser Aug 2000 A
6149653 Deslauriers Nov 2000 A
6152927 Farris et al. Nov 2000 A
6200330 Benderev et al. Mar 2001 B1
6206881 Frigg et al. Mar 2001 B1
D443060 Benirschke et al. May 2001 S
6270499 Leu et al. Aug 2001 B1
D449692 Michelson Oct 2001 S
6302887 Spranza et al. Oct 2001 B1
6331179 Freid et al. Dec 2001 B1
6348052 Sammarco Feb 2002 B1
6358250 Orbay Mar 2002 B1
6364881 Apgar et al. Apr 2002 B1
6364882 Orbay Apr 2002 B1
6379359 Dahners Apr 2002 B1
6398783 Michelson Jun 2002 B1
6406478 Kuo Jun 2002 B1
6409768 Tepic et al. Jun 2002 B1
6413259 Lyons et al. Jul 2002 B1
6440135 Orbay et al. Aug 2002 B2
6468278 Muckter Oct 2002 B1
6572620 Schon et al. Jun 2003 B1
6620195 Goble et al. Sep 2003 B2
6623486 Weaver et al. Sep 2003 B1
6663669 Reiley Dec 2003 B1
6669701 Steiner et al. Dec 2003 B2
6695844 Bramlet et al. Feb 2004 B2
6706046 Orbay et al. Mar 2004 B2
6712820 Orbay Mar 2004 B2
6719759 Wagner et al. Apr 2004 B2
6730090 Orbay et al. May 2004 B2
6776781 Uwaydah Aug 2004 B1
6863671 Strobel et al. Mar 2005 B1
6866665 Orbay Mar 2005 B2
6916323 Kitchens Jul 2005 B2
6945973 Bray Sep 2005 B2
7001388 Orbay et al. Feb 2006 B2
7063701 Michelson Jun 2006 B2
7128744 Weaver et al. Oct 2006 B2
D536453 Young et al. Feb 2007 S
7220246 Raulerson et al. May 2007 B2
7229444 Boyd Jun 2007 B2
7229445 Hayeck et al. Jun 2007 B2
7235079 Jensen et al. Jun 2007 B2
7354441 Frigg Apr 2008 B2
7500983 Kaiser et al. Mar 2009 B1
7563263 Orbay et al. Jul 2009 B2
7582107 Trail et al. Sep 2009 B2
7591823 Tipirneni Sep 2009 B2
7604657 Orbay et al. Oct 2009 B2
7637908 Gonzalez-Hernandez Dec 2009 B1
7651517 Konieczynski et al. Jan 2010 B2
7655029 Niederberger et al. Feb 2010 B2
7695472 Young Apr 2010 B2
7722653 Young et al. May 2010 B2
7740648 Young et al. Jun 2010 B2
7744638 Orbay Jun 2010 B2
7776076 Grady, Jr. et al. Aug 2010 B2
7780667 Watanabe et al. Aug 2010 B2
7780710 Orbay et al. Aug 2010 B2
7896886 Orbay et al. Mar 2011 B2
7909859 Mosca et al. Mar 2011 B2
7914532 Shaver et al. Mar 2011 B2
7927341 Orbay et al. Apr 2011 B2
7938850 Orbay et al. May 2011 B2
7951176 Grady et al. May 2011 B2
7951178 Jensen May 2011 B2
7955364 Ziolo et al. Jun 2011 B2
D643121 Milford et al. Aug 2011 S
8021402 Martin et al. Sep 2011 B2
D646785 Milford Oct 2011 S
8062296 Orbay et al. Nov 2011 B2
8062367 Kirschman Nov 2011 B2
8100953 White et al. Jan 2012 B2
8182485 Gonzalez-Hernandez May 2012 B1
8317842 Graham et al. Nov 2012 B2
8361075 Gonzalez-Hernandez Jan 2013 B2
8469999 Gonzalez-Hernandez Jun 2013 B2
8523902 Heaven et al. Sep 2013 B2
8556946 Prandi Oct 2013 B2
8574234 Gonzalez-Hernandez Nov 2013 B2
8597363 Liverneaux et al. Dec 2013 B2
8603091 Lutz Dec 2013 B2
8608783 Graham Dec 2013 B2
8690916 Gonzalez-Hernandez Apr 2014 B2
8728126 Steffen May 2014 B2
8764808 Gonzalez-Hernandez Jul 2014 B2
8870963 Gonzalez-Hernandez Oct 2014 B2
8906070 Medoff Dec 2014 B2
8961573 Gonzalez-Hernandez Feb 2015 B2
20020091391 Cole et al. Jul 2002 A1
20020165614 Tornier Nov 2002 A1
20030135212 Chow Jul 2003 A1
20030135216 Sevrain Jul 2003 A1
20030208210 Dreyfuss et al. Nov 2003 A1
20040097939 Bonutti May 2004 A1
20040193278 Maroney et al. Sep 2004 A1
20040199258 Macara Oct 2004 A1
20040210220 Tornier Oct 2004 A1
20050004574 Muckter Jan 2005 A1
20050015089 Young et al. Jan 2005 A1
20050021033 Zeiler et al. Jan 2005 A1
20050038513 Michelson Feb 2005 A1
20050085819 Ellis et al. Apr 2005 A1
20050182405 Orbay et al. Aug 2005 A1
20050240187 Huebner et al. Oct 2005 A1
20050267476 Chervitz et al. Dec 2005 A1
20050288681 Klotz et al. Dec 2005 A1
20060015072 Raulerson Jan 2006 A1
20060015101 Warburton et al. Jan 2006 A1
20060058795 Boyd Mar 2006 A1
20060106385 Pennig May 2006 A1
20060161156 Orbay Jul 2006 A1
20060217722 Dutoit et al. Sep 2006 A1
20060229623 Bonutti et al. Oct 2006 A1
20060235400 Scheider Oct 2006 A1
20060241617 Holloway et al. Oct 2006 A1
20060264947 Orbay et al. Nov 2006 A1
20060264949 Kohut Nov 2006 A1
20060264956 Orbay et al. Nov 2006 A1
20060271105 Foerster et al. Nov 2006 A1
20070005074 Chudik Jan 2007 A1
20070016205 Beutter et al. Jan 2007 A1
20070083207 Ziolo et al. Apr 2007 A1
20070123880 Medoff May 2007 A1
20070123885 Kirschman May 2007 A1
20070162015 Winquist et al. Jul 2007 A1
20070167953 Prien et al. Jul 2007 A1
20070233113 Kaelblein Oct 2007 A1
20070233114 Bouman Oct 2007 A1
20070233115 Sixto et al. Oct 2007 A1
20070265631 Fox Nov 2007 A1
20080015593 Pfefferle et al. Jan 2008 A1
20080045960 Bruecker et al. Feb 2008 A1
20080119895 Manceau May 2008 A1
20080132955 Frigg Jun 2008 A1
20080140130 Chan et al. Jun 2008 A1
20080154311 Staeubli Jun 2008 A1
20080161853 Arnold et al. Jul 2008 A1
20080161860 Ahrens et al. Jul 2008 A1
20080161863 Arnold et al. Jul 2008 A1
20080221577 Elghazaly Sep 2008 A1
20080234749 Forstein Sep 2008 A1
20080234752 Dahners Sep 2008 A1
20080249572 Tandon Oct 2008 A1
20090012571 Perrow et al. Jan 2009 A1
20090024173 Reis, Jr. Jan 2009 A1
20090048681 Vlachos Feb 2009 A1
20090069851 Gillard Mar 2009 A1
20090076554 Huebner et al. Mar 2009 A1
20090105838 Russo et al. Apr 2009 A1
20090118769 Sixto, Jr. May 2009 A1
20090125070 Sixto, Jr. et al. May 2009 A1
20090171399 White et al. Jul 2009 A1
20090192550 Leung et al. Jul 2009 A1
20090216270 Humphrey Aug 2009 A1
20090228010 Gonzalez-Hernandez et al. Sep 2009 A1
20090254089 Tipirneni et al. Oct 2009 A1
20090254189 Scheker Oct 2009 A1
20090264936 Gonzalez-Hernandez et al. Oct 2009 A1
20090275987 Graham et al. Nov 2009 A1
20090275991 Medoff Nov 2009 A1
20090281577 Graham et al. Nov 2009 A1
20090281578 Spencer Nov 2009 A1
20090299369 Orbay et al. Dec 2009 A1
20090306711 Stone et al. Dec 2009 A1
20090312758 Petit Dec 2009 A1
20090312760 Forstein et al. Dec 2009 A1
20090312802 Dasilva Dec 2009 A1
20090326591 Spencer, Jr. Dec 2009 A1
20100030276 Huebner et al. Feb 2010 A1
20100057086 Price et al. Mar 2010 A1
20100094358 Moore Apr 2010 A1
20100145339 Steffen Jun 2010 A1
20100145397 Overes et al. Jun 2010 A1
20100198258 Heaven et al. Aug 2010 A1
20100217393 Theofilos Aug 2010 A1
20100262194 Wagner et al. Oct 2010 A1
20100324602 Huebner et al. Dec 2010 A1
20100331844 Ellis et al. Dec 2010 A1
20110066153 Orbay Mar 2011 A1
20110152943 Gonzalez-Hernandez Jun 2011 A1
20110160730 Schonhardt et al. Jun 2011 A1
20110295324 Donley Dec 2011 A1
20120226321 Gonzalez-Hernandez Sep 2012 A1
20120226322 Gonzalez-Hernandez Sep 2012 A1
20120226323 Gonzalez-Hernandez Sep 2012 A1
20130096629 Rollinghoff et al. Apr 2013 A1
20130116734 Gonzalez-Hernandez May 2013 A1
20130338780 Berchoux et al. Dec 2013 A1
20140121709 Gonzalez-Hernandez May 2014 A1
20140121779 Gonzalez-Hernandez May 2014 A1
20140172020 Gonzalez-Hernandez Jun 2014 A1
20140180344 Gonzalez-Hernandez Jun 2014 A1
20140277177 Gonzalez-Hernandez Sep 2014 A1
20150164566 Gonzalez-Hernandez Jun 2015 A1
20200030104 Graham Jan 2020 A1
Foreign Referenced Citations (18)
Number Date Country
86 28 766 Dec 1986 DE
89 07 443 Sep 1989 DE
43 43 117 Jun 1995 DE
198 57 279 Jun 2000 DE
299 07 161 Aug 2000 DE
0 551 588 Nov 1992 EP
1 132 052 Sep 2001 EP
1 468 655 Oct 2004 EP
2 606 268 May 1988 FR
2 680 673 Mar 1993 FR
2 712 173 May 1995 FR
4-138152 May 1992 JP
WO 9938448 Aug 1999 WO
WO 02071963 Sep 2002 WO
WO 2005037117 Apr 2005 WO
WO 2008007194 Jan 2008 WO
WO 2008007196 Jan 2008 WO
WO 2012003884 Jan 2012 WO
Non-Patent Literature Citations (26)
Entry
Acumed; ACU-LOC Wrist Plating System; Jul. 2009; 20 pages.
Acumed; The Mayo Clinic Congruent Elbow Plates (catalog); 2003; 19 pages.
Acumed; The Mayo Clinic Congruent Elbow Plate System (catalog); Apr. 2006; 20 pages.
Christie, J., C.R. Howie and P.C. Armour, Fixation of displaced subcapital femoral fractures. Compression screw fixation versus double divergent pins. J Bone Joint Surg [Br ]1988; 70-B: 199-201.
Cross, W.M. et al., “Achieving stable fixation: biomechanical designs for fracture healing,” AAOS Now (2008) 3 pages.
Guha, AR, et al.; “A New Technique of Fixation of Radial Head Fractures Using a Modified Tubular Plate,” Journal of Postgraduate Medicine; Jul. 2004; vol. 50, Issue 2; pp. 113-114; Accessed Aug. 6, 2008 at: http://www.jpgmonline.com/article.asp?issn=0022-3859;year=2004;volume=50;issue=2;spage=113;epage=114;aulast=Guha.
Hand Innovations, LLC; DVR Anatomic, Volar Plating System; 2007; 4 pages.
Hussain M., R.N. Natarajan, A.H. Fayyazi, B.R. Braaksma, G.B. Andersson and H.S. An, Screw angulation affects bone-screw stresses and bone graft load sharing in an anterior cervical corpectomy fusion with a rigid screw-plate construct: a finite element model study; Spine Journal, vol. 9, Issue 12; Dec. 2009; pp. 1016-1023 (published online Oct. 12, 2009).
Lakatos, R. et al.; “General principles of internal fixation”; eMedicine; Aug. 2006; 51 pages.
“MIS Technique,” published by Zimmer®, 1 page, prior to Nov. 19, 2004.
Postak, Paul D.; “Biomechanical Properties of Fixed-Angle Volar Distal Radius Plates Under Dynamic Loading;” 2007; 6 pages.
Robert, III, K.Q., R. Chandler, R,V, Barratta, K.A. Thomas and M.B. Harris, The effect of divergent screw placement on the initial strength of plate-to-bone fixation. J Trauma. Dec. 2003;55(6):1139-44.
Synthes, “Large Fragment LCP Instrument and Implant Set;” technique guide; 2003; 31 pages.
Synthes; 3.5 mm LCP Periarticular Proximal Humerus Plate; Apr. 2010; 22 pages.
Synthes; Locking Compression Plate (LCP) System (brochure); 2003; 6 pages.
Synthes, “Locking Compression Plate (LCP) System. Locking screw technology and conventional plating in one system;” 2003; 6 pages.
Synthes; Locking Compression Plate (LCP) System (brochure); Jan. 2007; 6 pages.
Synthes; Modular Mini Fragment LCP System (brochure); 2007; 12 pages.
Synthes; Small Fragment Locking Compression Plate (LCP) System (brochure); 2002; 43 pages.
Written Opinion of the International Searching Authority; International Application No. PCT/US2009/036211; dated Sep. 23, 2010; 8 pages.
“Zimmer® Universal Locking System,” The Journal of Bone and Joint Surgery, vol. 89, No. 7, Jul. 2007, 1 page.
Zimmer, Inc. “Zimmer® Universal Locking System,” brochure (2006), 4 pages.
Zimmer, Inc.; “Zimmer Universal Locking System;” brochure; 2009, 2 pages.
Zimmer, Inc. “Zimmer Holdings to Launch Innovative Locking Plate System at Orthopaedic Trauma Association Meeting,” Sep. 14, 2006; 3 pages.
Zimmer, Inc.; “Zimmer Small Fragment Universal Locking System;” Surgical Technique; 2010; 16 pages.
Zimmer; Zimmer Periarticular Plating System-Low-Profile Fixation (catalog); 2003; 8 pages.
Related Publications (1)
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20200121466 A1 Apr 2020 US
Provisional Applications (1)
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61407072 Oct 2010 US
Divisions (3)
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Parent 15702006 Sep 2017 US
Child 16724433 US
Parent 14522702 Oct 2014 US
Child 15702006 US
Parent 13282810 Oct 2011 US
Child 14522702 US