Posterior prosthetic intervertebral disc

Information

  • Patent Grant
  • 11413156
  • Patent Number
    11,413,156
  • Date Filed
    Thursday, March 19, 2020
    4 years ago
  • Date Issued
    Tuesday, August 16, 2022
    a year ago
Abstract
A prosthetic intervertebral disc is formed of first and second end plates sized and shaped to fit within an intervertebral space and to be implanted from the back of the patient, thereby decreasing the invasiveness of the procedure. The posterior approach provides for a smaller posterior surgical incision and avoids important blood vessels located anterior to the spine particularly for lumbar disc replacements. The first and second plates are each formed of first, second and third parts are arranged in a first configuration in which the parts are axially aligned to form a low profile device appropriate for insertion through the small opening available in the TLIF or PLIF approaches described above. The three parts of both of the plates rotate and translate with respect to one another in situ to a second configuration or a deployed configuration in which the parts are axially unaligned with each other to provide a maximum coverage of the vertebral end plates for a minimum of insertion profile. Upon deployment of the disc, a height of the disc is increased.
Description
BACKGROUND OF THE INVENTION

The present invention relates to medical devices and methods. More specifically, the invention relates to intervertebral prosthetic discs and methods of preserving limited motion upon removal of an intervertebral disc.


Back pain takes an enormous toll on the health and productivity of people around the world. According to the American Academy of Orthopedic Surgeons, approximately 80 percent of Americans will experience back pain at some time in their life. In the year 2000, approximately 26 million visits were made to physicians' offices due to back problems in the United States. On any one day, it is estimated that 5% of the working population in America is disabled by back pain.


One common cause of back pain is injury, degeneration and/or dysfunction of one or more intervertebral discs. Intervertebral discs are the soft tissue structures located between each of the thirty-three vertebral bones that make up the vertebral (spinal) column. Essentially, the discs allow the vertebrae to move relative to one another. The vertebral column and discs are vital anatomical structures, in that they form a central axis that supports the head and torso, allow for movement of the back, and protect the spinal cord, which passes through the vertebrae in proximity to the discs.


Discs often become damaged due to wear and tear or acute injury. For example, discs may bulge (herniate), tear, rupture, degenerate or the like. A bulging disc may press against the spinal cord or a nerve exiting the spinal cord, causing “radicular” pain (pain in one or more extremities caused by impingement of a nerve root). Degeneration or other damage to a disc may cause a loss of “disc height,” meaning that the natural space between two vertebrae decreases. Decreased disc height may cause a disc to bulge, facet loads to increase, two vertebrae to rub together in an unnatural way and/or increased pressure on certain parts of the vertebrae and/or nerve roots, thus causing pain. In general, chronic and acute damage to intervertebral discs is a common source of back related pain and loss of mobility.


When one or more damaged intervertebral disc cause a patient pain and discomfort, surgery is often required. Traditionally, surgical procedures for treating intervertebral discs have involved discectomy (partial or total removal of a disc), with or without interbody fusion of the two vertebrae adjacent to the disc. When the disc is partially or completely removed, it is necessary to replace the excised disc material with natural bone or artificial support structures to prevent direct contact between hard bony surfaces of adjacent vertebrae. Oftentimes, pins, rods, screws, cages and/or the like arc inserted between the vertebrae to act as support structures to hold the vertebrae and any graft material in place while the bones permanently fuse together.


A more recent alternative to traditional fusion is total disc replacement or TDR. TDR provides the ability to treat disc related pain without fusion provided by bridging bone, by using a movable, implantable, artificial intervertebral disc (or “disc prosthesis”) between two vertebrae. A number of different artificial intervertebral discs are currently being developed. For example, U.S. Patent Application Publication Nos. 2005/0021146, 2005/0021145, and 2006/0025862, which are hereby incorporated by reference in their entirety, describe artificial intervertebral discs with mobile bearing designs. Other examples of intervertebral disc prostheses are the LINK® SB Charite disc (provided by DePuy Spine, Inc.) MOBIDISC® (provided by LDR Medical (www.ldrmedical.fr)), the BRYAN Cervical Disc (provided by Medtronic Sofamor Danek, Inc.), the PRODISC® or PRODISC-C® (from Synthes Stratec, Inc.), the PCM disc (provided by Cervitech, Inc.), and the MAVERICK® disc (provided by Medtronic Sofomor Danek).


A potential drawback of these known disc designs is that the prosthetic disc must be inserted from the anterior side of the patient. The anterior approach can be difficult and may require a vascular surgeon as the prosthetic disc passes near important blood vessels located anterior to the spine. Other currently available intervertebral disc prostheses usually have similar drawbacks, including invasiveness of the surgery and/or surgical skill and complexity.


Another prosthetic approach has been to fuse the vertebrae, for example with transforaminal lumbar interbody fusion (TLIF) surgery or posterior lumbar interbody fusion (PLIF) surgery. These procedures allow the surgery to be performed from the posterior without passing through the abdominal cavity and the associated drawbacks. The TLIF or PLIF approaches involve passing through a much smaller space than an anterior approach and generally require at least partial removal of one or more facet joints to provide enough space for access to the disc space. It is this limitation on space that has until now prevented the design of a successful artificial disc for delivery by a TLIF or PLIF approach.


Therefore, a need exists for an improved disc for preserving motion and maintaining disc spacing between two vertebrae after removal of an intervertebral disc which can be delivered by a TLIF or PLIF approach. Ideally, such improved disc would be introduced in a small configuration and expanded in vivo to a larger configuration.


BRIEF SUMMARY OF THE INVENTION

Embodiments of the present invention provide a prosthetic intervertebral disc which is implanted from a PLIF or TLIF approach and is deployed from a small insertion configuration to a larger deployed configuration in vivo.


In accordance with one aspect of the invention, a prosthetic intervertebral disc includes first and second end plates sized and shaped to fit within an intervertebral space, each end plate having a vertebral contacting surface and an inner surface and a first bearing surface on an inner surface of the first end plate and a second bearing surface on an inner surface of the second end plate. The first and second bearing surfaces are arranged to allow articulation and rotation between the first and second plates. The first and second plates are each formed of first, second and third parts having a first configuration in which the parts are axially aligned to a second configuration in which the parts are axially unaligned with each other. The first and second plates are deployed in situ from the first configuration to the second configuration by both rotation and sliding of the parts over one another. The deployment from the first configuration to the second configuration increases a height of the disc.


In accordance with another embodiment of the invention, a prosthetic intervertebral disc includes first and second end plates sized and shaped to fit within an intervertebral space, each end plate having a vertebral contacting surface and an inner surface, a first bearing surface on an inner surface of the first end plate and a second bearing surface on an inner surface of the second end plate, the first and second bearing surfaces opposed to one another, and a mobile core configured to be received between the first and second bearing surfaces and arranged to allow articulation and rotation between the first and second plates. The first and second plates are each formed of first, second and third parts having a first configuration in which the parts are axially aligned and a second configuration in which the parts are axially unaligned with each other. A track is formed in the first and second end plates. The track is configured to allow the mobile core to move from a first position outside of the bearing surfaces to a position between the bearing surfaces, wherein the movement of the mobile core from the first position to the second position increases a height of the disc.


In accordance with a further aspect of the invention, a method of deploying a prosthetic intervertebral disc comprises the steps of: providing a prosthetic intervertebral disc having first and second end plates each having a vertebral contacting surface and an inner surface, a first bearing surface on an inner surface of the first end plate and a second bearing surface on an inner surface of the second end plate, the first and second bearing surfaces arranged to allow articulation and rotation between the first and second plates, wherein the first and second plates are each formed of first, second and third parts; inserting the intervertebral disc between two vertebrae in a configuration in which the first, second and third parts of each of the plates are axially aligned; and deploying the first and second plates in situ from the first configuration to a second configuration in which the parts are axially unaligned with each other by both rotation and sliding of the parts over one another, wherein the deployment from the first configuration to the second configuration increases a height of the disc. In accordance with an additional aspect of the invention, a method of deploying a prosthetic intervertebral disc includes the steps of: providing a prosthetic intervertebral disc comprising first and second end plates and a mobile core arranged to allow articulation and rotation between the first and second plates, wherein the first and second plates are each formed of first, second and third parts; inserting the intervertebral disc between two vertebrae in a configuration in which the first, second and third parts of each of the plates are substantially axially aligned; deploying the first and second plates in situ from the first configuration to a second configuration in which the parts are axially unaligned with each other; and moving the mobile core along a track between the end plates, wherein the movement of the mobile core from the first position to the second position increases a height of the disc.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a perspective view of a posterior prosthetic intervertebral disc in a narrow insertion configuration;



FIG. 2 is a side view of the disc of FIG. 1;



FIG. 3 is a top view of the disc of FIG. 1;



FIG. 4 is a side cross sectional view of the disc of FIG. 1 taken along the line 4-4 of FIG. 3;



FIG. 5 is a cross sectional view of the disc of FIG. 1 taken along the line 5-5 of FIG. 2;



FIG. 6 is a perspective view of the disc of FIG. 1 is an expanded deployed configuration;



FIG. 7 is a top view of the deployed disc of FIG. 6;



FIG. 8 is a top view of an alternative embodiment of a posterior prosthetic intervertebral disc in a partially deployed configuration;



FIG. 9 is a perspective view of the disc of FIG. 8;



FIG. 10 is a side view of the disc of FIG. 8;



FIG. 11 is a perspective view of the disc of FIG. 8 with the core moving along a track from the position of FIG. 8 to the fully deployed position of FIG. 12; and



FIG. 12 is a perspective view of the disc of FIG. 8 with the core in a fully deployed position.





DETAILED DESCRIPTION OF THE INVENTION

The present invention provides an implanted intervertebral disc assembly which both restores motion and can be implanted from the back of the patient, thereby decreasing the invasiveness of the procedure. The posterior approach provides for a smaller posterior surgical incision and avoids important blood vessels located anterior to the spine particularly for lumbar disc replacements. The intervertebral discs described herein are designed to be suitable for either a PLIF or TLIF approach to the spine. These approaches require insertion of a device with a small insertion profile which can be expanded or assembled in vivo into a complete disc assembly.


PLIF stands for Posterior Lumbar Interbody Fusion. In the PLIF approach to the spine, the vertebrae arc reached through an incision in the patient's back (posterior). The PLIF procedure involves forming a 3-6 inch incision in the patient's back and retracting the spinal muscles to allow access to the vertebral disc. The surgeon then carefully removes the lamina (laminectomy) to be able to see and access the nerve roots. The facet joints, which lie directly over the nerve roots, may be trimmed to allow more room for the nerve roots. Depending on the amount of space available, ¼ to ½ of the facets may be removed. The surgeon then removes some or all of the affected disc and surrounding tissue. Once the disc space is prepared, hardware, such as an intervertebral disc, is inserted into the disc space. The space available for insertion of the intervertebral disc can vary depending on the patient, but generally the opening has a width and height of about 1 cm which with distraction can form a slightly larger opening.


TLIF stands for Transforaminal Lumbar Interbody Fusion. The TLIF has recently gained popularity as a surgical access to the lumbar spine and provides some potential advantages over the PLIF approach. The TLIF technique involves approaching the spine in a similar manner as the PLIF approach but more from the side of the spinal canal through a midline incision in the patients back. This approach greatly reduces the amount of surgical muscle dissection and minimizes the nerve manipulation required to access the vertebrae, discs and nerves. The TLIF approach is generally less traumatic to the spine, is safer for the nerves, and allows for minimal access. However, the TLIF involves the removal of at least one and possibly both facets.



FIG. 1 illustrates a prosthetic intervertebral disc 10 formed of first and second end plates 12, 14 sized and shaped to fit within an intervertebral space. Each plate 12, 14 has a vertebral contacting outer surface 16 and an inner surface carrying first and second bearing surfaces 18, 20 (shown in FIGS. 4 and 5). The first bearing surface 18 in the embodiment of FIG. 1 is a concave bearing surface while the second bearing surface 20 is a mating convex bearing surface. Together the bearing surfaces 18, 20 form a ball and socket joint arranged to allow articulation and rotation between the first and second plates 12, 14.


The first and second plates 12, 14 are each formed of first, second and third parts 22, 24, 26. The three parts 22, 24, 26 have a first configuration, shown in FIG. 1 in which the parts are axially aligned to form a low profile device appropriate for insertion through the small opening available in the TLIF or PLIF approaches described above. Preferably, the undeployed configuration of FIG. 1 has a height less than about 10 mm and a width less than about 12 mm. The three parts 22, 24, 26 of both of the plates 12, 14 rotate and translate with respect to one another in situ to a second configuration or a deployed configuration in which the parts are axially unaligned with each other. In the deployed configuration, as shown in FIGS. 6 and 7, the three parts form a substantially H-shaped configuration which provides a maximum coverage of the vertebral end plates for a minimum of insertion profile. As the three parts 22, 24, 26 translate with respect to one another to the deployed configuration a height of the disc is increased in a manner which will be described in detail below.


The bone integration surfaces 16 of the disc 10 have been shown as flat surfaces for ease of illustration. The outer vertebral body contacting surface 16 may take on any of the configurations known in the art. Oftentimes, the outer surfaces 16 will include one or more surface features and/or materials to enhance attachment of the disc 10 to vertebral bone. For example, the outer surfaces 16 may be machined to have serrations, teeth or other surface features for promoting adhesion of the plates 12, 14 to a vertebra. In one embodiment, serrations are provided on the outer surfaces 16. The serrations can be pyramid shaped serrations extending in mutually orthogonal directions, but other geometries of serrations or other features including teeth, grooves, ridges, pins, barbs and combinations thereof would also be useful. When the bone integration structures are ridges, teeth, barbs or similar structures, they may be angled to ease insertion and prevent migration. The outer surfaces may include other fixation means inserted after deployment of the disc 10, including one or more fins, pins, or screws. In one embodiment, one or more fins are provided on the last of the three parts to enter the disc space. Optionally, additional fins may be provided that are inserted after the disc is positioned by sliding the fin(s) into one or more slots in the endplates.


The outer surfaces 16 may be provided with a rough microfinish formed by blasting with aluminum oxide microparticles or the like to improve bone integration. In some embodiments, the outer surface 16 may also be titanium plasma sprayed or HA coated to further enhance attachment of the outer surface to vertebral bone.


The disc 10 may be deployed with the aid of various instruments including one or more distracters, sizing guides, placement instruments and deployment instruments. The deployment instruments can be fixed to the ends of the disc 10 in the insertion configuration shown in FIG. 1 by a connection means, such as a quick connect or a threaded coupling. The placement and deployment instruments generally include at least two instruments with one instrument inserted though each of the two openings formed at the posterior side of the disc space on either side of the spine. Referring now to FIG. 3, the sequence of deployment of the disc 10 includes rotation of the first and third parts 22, 26 with respect to the second part 24 in the direction of the arrows A, followed by sliding of the second part 24 along first and third parts in the direction of the arrow B to form the deployed configuration shown in FIGS. 6 and 7.


The disc 10 includes cylindrical pegs 30 on opposite ends of the second parts 24 which fit into channels 32 on the first and third parts 22, 26 to allow first rotation and then translation of the second part along the first and third parts. The rotation of the disc 10 from the substantially linear arrangement of FIGS. 1-3 to a substantially U-shaped arrangement (not shown) can be caused by contact of a leading end of the inserted disc with an annulus of the natural disc. The U-shaped configuration is then converted to the final H-shaped configuration by pulling the second part 24 posteriorly in the direction of the arrow B. The sliding of the second or center part 24 along the channels 32 causes the disc space to be distracted, i.e. the height of the disc increases from an initial height H.sub.i, shown in FIG. 2 to a deployed height H.sub.d, shown in FIG. 6. This distraction or separation of the end plates is provided by ramps 34 which lie along each side of the channel 32 in the first and third parts 22, 26. The deployed height H.sub.d is preferably between 1.3 and 2 times the initial height H. In one example, the deployed height H.sub.d is about 1.5 times the initial height H.sub.i and provides a final deployed disc configuration shown in FIG. 6 which is significantly higher than the height of the access opening provided by the posterior PLIF or TLIF approach.


Another embodiment of a posterior prosthetic intervertebral disc 100 is shown in FIGS. 8-12. The prosthetic disc 100 includes first and second end plates 112, 114 sized and shaped to fit within an intervertebral space, each end plate having a vertebral contacting surface 116 and an opposite inner surface including a bearing surface 118. The disc 100 includes a mobile core 120 which in a deployed configuration is positioned between the opposing bearing surfaces 118 to provide a mobile core articulating disc design. As in the embodiment of FIG. 1, each of the plates 12, 114 are formed of first, second and third parts 122, 124, 126. The three parts of the plates have a first configuration for insertion of the disc 100 through a small posterior keyhole into the disc space. In the first configuration (not shown) the three parts 122, 124, 126 are substantially axially aligned. The after insertion, the three parts 122, 124, 126 are rotated by pivoting on interconnecting posts 130 to a second configuration in which the parts are axially unaligned with each other and arranged with the first and third parts 122, 126 at an angle of about 20-90 degrees with respect to one another, preferably about 70-85 degrees.


The mobile core 120 includes opposite convex bearing surfaces arranged to be received between the first and second bearing surfaces 118 of the plates to allow articulation, rotation and some translation between the first and second plates. As shown in FIGS. 8-10, for insertion of the disc 100 into the disc space, the core 120 is positioned in a seat 132 formed between the first parts 122 at one end of the first parts. After insertion of the disc 100 into the disc space, the core 120 is advanced along a track 134, shown in FIG. 11 from the seat 132 to a final deployed position between the bearing surfaces 118 of the plates. FIG. 12 shows the core 120 seated between the bearing surfaces 118. The bearing surfaces 118 may include one or more core retaining features, such as a retaining ring or other peripheral retaining features. As can be seen in FIG. 11, the movement of the mobile core 130 from the first position in the seat 132 to the second position between the bearing surfaces 118 distracts the plates 112, 114 away from one another and increases a height of the disc 100 from an initial height H.sub.i, shown in FIG. 10 to a deployed height H.sub.d shown in FIG. 12.


The procedure for replacing a natural intervertebral disc with the artificial intervertebral discs 10, 100 includes using a PLIF or TLIF approach to the spine, by forming a 3-6 inch incision in the patient's back and retracting the spinal muscles to allow access to the vertebral disc. The surgeon then carefully removes the lamina (laminectomy) to be able to see and access the nerve roots. The disc space is then entered through a preexisting opening or through an opening formed by cutting away a portion of or an entire one or more facet. Those skilled in the art will understand the procedure of preparing the disc space and implanting the disc which is summarized herein. A far posterio-lateral minimally invasive approach can be used so as to allow for the minimum of facet removal such that the facet joints remain substantially intact. The surgeon then removes some or all of the affected disc and surrounding tissue. Once the disc space is prepared the intervertebral disc is inserted into the disc space in the insertion configuration in which the first, second and third parts are aligned. The space available for insertion of the intervertebral disc can vary depending on the patient, but generally the opening has a width and height of about 1 cm which with distraction can form a slightly larger opening, i.e. about 1 cm by 1.2 cm. The deployment of the discs 10, 100 can be performed through a single posterior opening, or preferably, through two posterior openings to allow the surgeon better access to deploy the disc. In one embodiment, one of the two openings is used for insertion of the disc while the other opening is used for a distraction instrument and/or other deployment instruments.


The upper and lower plates 12, 14, 112, 114 may be constructed from any suitable metal, alloy or combination of metals or alloys, such as but not limited to cobalt chrome alloys, titanium (such as grade 5 titanium), titanium based alloys, tantalum, nickel titanium alloys, stainless steel, and/or the like. They may also be formed of ceramics, biologically compatible polymers including PEEK, UHMWPE, PLA or fiber reinforced polymers. The plates 12, 14, 112, 114 may be formed of a one piece construction or may be formed of more than one piece, such as different materials coupled together.


The core 130 can be made of low friction materials, such as titanium, titanium nitrides, other titanium based alloys, tantalum, nickel titanium alloys, stainless steel, cobalt chrome alloys, ceramics, or biologically compatible polymer materials including PEEK, UHMWPE, PLA or fiber reinforced polymers. High friction coating materials can also be used.


Different materials may be used for different parts of the disc 10 to optimize imaging characteristics. PEEK plates may also be coated with titanium plasma spray or provided with titanium screens for improved bone integration. Other materials and coatings can also be used such as titanium coated with titanium nitride, aluminum oxide blasting, HA (hydroxylapatite) coating, micro HA coating, and/or bone integration promoting coatings. Any other suitable metals or combinations of metals may be used as well as ceramic or polymer materials, and combinations thereof. Any suitable technique may be used to couple materials together, such as snap fitting, slip fitting, lamination, interference fitting, use of adhesives, welding and the like.


Although the present invention has been described as having a ball in socket design (disc 10) or a mobile core design (disc 100), the articulation surfaces may be varied to take on any of the different articulation designs known in the art. For example, the disc 10 may use a mobile bearing design in place of the ball and socket articulation. In one alternative embodiment of the invention non-symmetrically shaped bearing surfaces are used to tailor the articulation of the disc to the anatomy. In one example, the bearing surfaces are arranged to allow a maximum of 12 degrees of motion in flexion, a maximum of 8 degrees in extension and a maximum of 8 degrees in each direction of lateral bending. This configuration is useful particularly in the lumbar spine where the average range of motion of the various segments is larger in flexion that in extension or lateral bending.


Although the core 130 of FIG. 8 has been shown as circular in cross section with spherically shaped bearing surfaces, other shapes may be used including oval, elliptical, or kidney bean shaped. The circular shaped core does not limit rotational motion between the plates. The non-circular shaped cores can be used to limit rotational motion between the upper and lower plates 112, 113. When the core 130 is formed of a polymer such as PEEK which is invisible under radiographic imaging, it may be desirable to have a radiographic marker imbedded within the core.


While the exemplary embodiments have been described in some detail, by way of example and for clarity of understanding, those of skill in the art will recognize that a variety of modifications, adaptations, and changes may be employed. Hence, the scope of the present invention should be limited solely by the appended claims.

Claims
  • 1. A prosthetic intervertebral disc comprising: first and second end plates sized and shaped to fit within an intervertebral space, each end plate having a vertebral contacting surface and an opposite inner surface;wherein the first and second end plates are each formed of at least two pivotably interconnected elongated parts having a first configuration in which the at least two elongated parts are pivoted relative to each other to be substantially axially aligned with each other in an insertion configuration and a second configuration in which the at least two elongated parts are pivoted relative to each other to be axially unaligned with each other in a deployed configuration, wherein the prosthetic intervertebral disc has a wider width in the deployed configuration than that in the insertion configuration;the inner surface of the first end plate includes a first bearing surface on one of the at least two pivotably interconnected elongated parts of the first end plate and the inner surface of the second end plate includes a second bearing surface on one of the at least two pivotably interconnected elongated parts of the second end plate, the first and second bearing surfaces opposed to one another;a mobile core configured to be received between the first and second bearing surfaces and arranged to allow articulation between the mobile core and each of the first and second end plates; anda track formed in the inner surfaces of the first and second end plates, the track is configured to allow the mobile core to slidably move therealong from a first position between the other of the at least two interconnected parts of the first and second end plates outside of the bearing surfaces to a second position between the bearing surfaces when the first and second end plates are in the deployed configuration, wherein the movement of the mobile core from the first position to the second position increases a height of the prosthetic intervertebral disc measured between the vertebral contacting surfaces of the first and second end plates, wherein in both the first position and the second position, the mobile core is positioned between the first and second end plates.
  • 2. The disc of claim 1, wherein the at least two elongated parts comprise first, second and third parts arranged with the second part interconnecting the first and third parts.
  • 3. The disc of claim 2, wherein the first and third parts are arranged to pivot on opposite ends of the second part during deployment.
  • 4. The disc of claim 1, wherein the insertion configuration comprises a substantially linear arrangement of the at least two elongated parts of each of the first and second end plates.
  • 5. The disc of claim 4, wherein the at least two elongated parts comprise first, second and third parts and the deployed configuration comprises a substantially H-shaped arrangement.
  • 6. The disc of claim 1, wherein the prosthetic intervertebral disc in the insertion configuration has the height less than 10 mm and the width less than 12 mm.
  • 7. The disc of claim 1, wherein the height of the prosthetic intervertebral disc when the mobile core is in the second position is at least 1.5 times the height of the prosthetic intervertebral disc when the mobile core is in the first position.
  • 8. The prosthetic intervertebral disc of claim 1, wherein the mobile core allows articulation of the end plates relative to each other in an anterior/posterior direction and in a lateral direction.
  • 9. A prosthetic intervertebral disc comprising: first and second end plates sized and shaped to fit within an intervertebral space, each end plate having a vertebral contacting surface and an opposite inner surface;wherein the first and second end plates are each formed of at least two elongated parts pivotably connected to each other by a post, said at least two elongated parts of each of the first and second end plates having a first configuration in which the at least two elongated parts are pivoted relative to each other to be substantially axially aligned with each other in an insertion configuration and a second configuration in which the at least two elongated parts are pivoted relative to each other to be axially unaligned with each other in a deployed configuration, wherein a width of the prosthetic intervertebral disc in the deployed configuration is greater than that in the insertion configuration;the inner surface of the first end plate includes a first bearing surface on one of the at least two elongated parts of the first end plate and the inner surface of the second end plate includes a second bearing surface on one of the at least two elongated parts of the second end plate, the first and second bearing surfaces opposed to one another;a mobile member configured to be received between the first and second bearing surfaces and arranged to articulate with respect to both the first and second bearing surfaces and to allow articulation between the first and second end plates; anda track formed in the inner surfaces of the first and second end plates, the track is configured to allow the mobile member to slidably move therealong from a first position between the other of the at least two elongated parts of the first and second end plates outside of the bearing surfaces to a second position between the bearing surfaces when the first and second end plates are in the deployed configuration, wherein the movement of the mobile member from the first position to the second position increases a height of the prosthetic intervertebral disc measured between the vertebral contacting surfaces of the first and second end plates, wherein in both the first position and the second position, the mobile member is positioned between the first and second end plates.
  • 10. The disc of claim 9, wherein the at least two elongated parts comprise first, second and third parts arranged with the second part interconnecting the first and third parts.
  • 11. The disc of claim 10, wherein the first and third parts are arranged to pivot on opposite ends of the second part during deployment.
  • 12. The disc of claim 9, wherein the insertion configuration comprises a substantially linear arrangement of the at least two elongated parts of each of the first and second end plates.
  • 13. The disc of claim 12, wherein the at least two elongated parts comprise first, second and third parts and the deployed configuration comprises a substantially H-shaped arrangement.
  • 14. The disc of claim 9, wherein the prosthetic intervertebral disc in the insertion configuration has the height less than 10 mm and the width less than 12 mm.
  • 15. The disc of claim 9, wherein the height of the prosthetic intervertebral disc when the mobile member is in the second position is at least 1.5 times the height of the prosthetic intervertebral disc when the mobile member is in the first position.
  • 16. The prosthetic intervertebral disc of claim 9, wherein the mobile member allows articulation of the end plates relative to each other in an anterior/posterior direction and in a lateral direction.
CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 15/144,689, filed May 2, 2016, which is a divisional of U.S. patent application Ser. No. 14/467,274, filed Aug. 25, 2014, now U.S. Pat. No. 9,351,846, which is a divisional of U.S. patent application Ser. No. 12/504,042, filed Jul. 16, 2009, now U.S. Pat. No. 8,845,730, which claims priority to U.S. Provisional Application No. 61/081,952, filed Jul. 18, 2008, the full disclosures of which is incorporated herein by reference.

US Referenced Citations (384)
Number Name Date Kind
3486505 Gordon Dec 1969 A
3867728 Stubstad et al. Feb 1975 A
4309777 Patil Jan 1982 A
4531917 Linkow et al. Jul 1985 A
4566466 Ripple et al. Jan 1986 A
4619660 Christiansen et al. Oct 1986 A
4673407 Martin Jun 1987 A
4759766 Buettner-Janz et al. Jul 1988 A
4759769 Hedman et al. Jul 1988 A
4834757 Brantigan May 1989 A
4863477 Monson Sep 1989 A
4904261 Dove et al. Feb 1990 A
4917704 Frey et al. Apr 1990 A
4932969 Frey et al. Jun 1990 A
4946378 Hirayama et al. Aug 1990 A
4997432 Keller et al. Mar 1991 A
5035716 Downey Jul 1991 A
5057108 Shetty et al. Oct 1991 A
5071437 Steffee Dec 1991 A
5122130 Keller Jun 1992 A
5195526 Michelson Mar 1993 A
5258031 Salib et al. Nov 1993 A
5282861 Kaplan Feb 1994 A
5314477 Marnay May 1994 A
5320644 Baumgartner Jun 1994 A
5370697 Baumgartner et al. Dec 1994 A
5394457 Leibinger et al. Feb 1995 A
5401269 Buettner-Janz et al. Mar 1995 A
5415704 Davidson May 1995 A
5458642 Beer et al. Oct 1995 A
5462575 Del Corso Oct 1995 A
5484437 Michelson Jan 1996 A
5489307 Kuslich et al. Feb 1996 A
5505732 Michelson Apr 1996 A
5507816 Bullivant Apr 1996 A
5534030 Navarro et al. Jul 1996 A
5556431 Büttner-Janz Sep 1996 A
5674296 Bryan et al. Oct 1997 A
5676701 Yuan et al. Oct 1997 A
5676702 Ratron Oct 1997 A
5683465 Shinn et al. Nov 1997 A
5702450 Bisserie Dec 1997 A
5709683 Bagby Jan 1998 A
5728159 Stroever et al. Mar 1998 A
5741253 Michelson Apr 1998 A
5776198 Rabbe et al. Jul 1998 A
5782832 Larsen et al. Jul 1998 A
5797909 Michelson Aug 1998 A
5824094 Serhan et al. Oct 1998 A
5865846 Bryan et al. Feb 1999 A
5865848 Baker Feb 1999 A
5888226 Rogozinski Mar 1999 A
5895428 Berry Apr 1999 A
5899901 Middleton May 1999 A
5899911 Carter May 1999 A
5928284 Mehdizadeh Jul 1999 A
5989251 Nichols Nov 1999 A
5989291 Ralph et al. Nov 1999 A
6001130 Bryan et al. Dec 1999 A
6019792 Cauthen Feb 2000 A
6022376 Assell et al. Feb 2000 A
6039761 Li et al. Mar 2000 A
6039763 Shelokov Mar 2000 A
6080155 Michelson Jun 2000 A
6083228 Michelson Jul 2000 A
6086613 Camino et al. Jul 2000 A
6096038 Michelson Aug 2000 A
6132465 Ray et al. Oct 2000 A
6136031 Middleton Oct 2000 A
6139551 Michelson et al. Oct 2000 A
6139579 Steffee et al. Oct 2000 A
6143033 Paul et al. Nov 2000 A
6146421 Gordon et al. Nov 2000 A
6156067 Bryan et al. Dec 2000 A
6159214 Michelson Dec 2000 A
6162252 Kuras et al. Dec 2000 A
6174311 Branch et al. Jan 2001 B1
6176881 Schaer et al. Jan 2001 B1
6193757 Foley et al. Feb 2001 B1
6224595 Michelson May 2001 B1
6224607 Michelson May 2001 B1
6231609 Mehdizadeh May 2001 B1
6235030 Zucherman et al. May 2001 B1
6261296 Aebi et al. Jul 2001 B1
6264695 Stoy Jul 2001 B1
6290726 Pope et al. Sep 2001 B1
6296664 Middleton Oct 2001 B1
6315797 Middleton Nov 2001 B1
6322567 Mittelstadt et al. Nov 2001 B1
6336941 Subba et al. Jan 2002 B1
6348071 Steffee et al. Feb 2002 B1
6368350 Erickson et al. Apr 2002 B1
6368351 Glenn et al. Apr 2002 B1
6375681 Truscott Apr 2002 B1
6375682 Fleischmann et al. Apr 2002 B1
6395032 Gauchet May 2002 B1
6402785 Zdeblick et al. Jun 2002 B1
6409766 Brett Jun 2002 B1
6413278 Marchosky Jul 2002 B1
6416551 Keller Jul 2002 B1
6436098 Michelson Aug 2002 B1
6440139 Michelson Aug 2002 B2
6447544 Michelson Sep 2002 B1
6478800 Fraser et al. Nov 2002 B1
6517544 Michelson Feb 2003 B1
6517580 Ramadan et al. Feb 2003 B1
6520967 Cauthen Feb 2003 B1
6520996 Manasas et al. Feb 2003 B1
6527804 Gauchet et al. Mar 2003 B1
6533817 Norton et al. Mar 2003 B1
6537279 Michelson Mar 2003 B1
6554863 Paul et al. Apr 2003 B2
6562047 Ralph et al. May 2003 B2
6562074 Gerbec et al. May 2003 B2
6565574 Michelson May 2003 B2
6582466 Gauchet Jun 2003 B1
6582468 Gauchet Jun 2003 B1
6592624 Fraser et al. Jul 2003 B1
6599294 Fuss et al. Jul 2003 B2
6607558 Kuras Aug 2003 B2
6607559 Ralph et al. Aug 2003 B2
6610092 Ralph et al. Aug 2003 B2
6623525 Ralph et al. Sep 2003 B2
6645248 Casutt Nov 2003 B2
6648895 Burkus et al. Nov 2003 B2
6652533 O'Neil Nov 2003 B2
6660038 Boyer et al. Dec 2003 B2
6666866 Martz et al. Dec 2003 B2
6669731 Ralph et al. Dec 2003 B2
6669732 Serhan et al. Dec 2003 B2
6673113 Ralph et al. Jan 2004 B2
6682562 Viart et al. Jan 2004 B2
6689132 Biscup Feb 2004 B2
6706068 Ferree Mar 2004 B2
6709439 Rogers et al. Mar 2004 B2
6712819 Zucherman et al. Mar 2004 B2
6712825 Aebi et al. Mar 2004 B2
6723097 Fraser et al. Apr 2004 B2
6726720 Ross et al. Apr 2004 B2
6726721 Stoy et al. Apr 2004 B2
6733532 Gauchet et al. May 2004 B1
6740118 Eisermann et al. May 2004 B2
6740119 Ralph et al. May 2004 B2
6755841 Fraser et al. Jun 2004 B2
6764515 Ralph et al. Jul 2004 B2
6770095 Grinberg et al. Aug 2004 B2
6790233 Brodke et al. Sep 2004 B2
6793678 Hawkins Sep 2004 B2
6814737 Cauthen Nov 2004 B2
6821298 Jackson Nov 2004 B1
6827740 Michelson Dec 2004 B1
6846328 Cauthen Jan 2005 B2
6863673 Gerbec et al. Mar 2005 B2
6875213 Michelson Apr 2005 B2
6896680 Michelson May 2005 B2
6899735 Coates et al. May 2005 B2
6936071 Marnay et al. Aug 2005 B1
6936132 Topolnitsky Aug 2005 B2
6964686 Gordon Nov 2005 B2
6966929 Mitchell Nov 2005 B2
6989011 Paul et al. Jan 2006 B2
6994727 Khandkar et al. Feb 2006 B2
7011684 Eckman Mar 2006 B2
7022138 Mashburn Apr 2006 B2
7025787 Bryan et al. Apr 2006 B2
7044983 Cheng May 2006 B1
7056344 Huppert et al. Jun 2006 B2
7060073 Frey et al. Jun 2006 B2
7066958 Ferree Jun 2006 B2
7081120 Li et al. Jul 2006 B2
7083651 Diaz et al. Aug 2006 B2
7087055 Lim et al. Aug 2006 B2
7097648 Globerman et al. Aug 2006 B1
7115132 Errico et al. Oct 2006 B2
7118580 Beyersdorff et al. Oct 2006 B1
7147665 Bryan et al. Dec 2006 B1
7153325 Kim et al. Dec 2006 B2
7179294 Eisermann et al. Feb 2007 B2
7182784 Evans et al. Feb 2007 B2
7198644 Schultz et al. Apr 2007 B2
7207991 Michelson Apr 2007 B2
7214244 Zubok et al. May 2007 B2
7217291 Zucherman et al. May 2007 B2
7235082 Bartish et al. Jun 2007 B2
7235103 Rivin Jun 2007 B2
7250060 Trieu Jul 2007 B2
7255714 Malek Aug 2007 B2
7261739 Ralph et al. Aug 2007 B2
7267688 Ferree Sep 2007 B2
7270679 Istephanous et al. Sep 2007 B2
7270682 Frigg et al. Sep 2007 B2
7303583 Schaer et al. Dec 2007 B1
7318839 Malberg et al. Jan 2008 B2
7326250 Beaurain et al. Feb 2008 B2
7331995 Eisermann et al. Feb 2008 B2
7429270 Baumgartner et al. Sep 2008 B2
7442211 De Villiers et al. Oct 2008 B2
7452380 Zubok et al. Nov 2008 B2
7491241 Errico et al. Feb 2009 B2
7494508 Zeegers et al. Feb 2009 B2
7531001 De Villiers et al. May 2009 B2
8303660 Abdou Nov 2012 B1
8808383 Kwak et al. Aug 2014 B2
8845730 De et al. Sep 2014 B2
9351846 De Villiers et al. May 2016 B2
9351852 Bao et al. May 2016 B2
10342670 De et al. Jul 2019 B2
20010016773 Serhan et al. Aug 2001 A1
20010029377 Aebi et al. Oct 2001 A1
20020022845 Zdeblick et al. Feb 2002 A1
20020035400 Bryan et al. Mar 2002 A1
20020045904 Fuss et al. Apr 2002 A1
20020068936 Burkus et al. Jun 2002 A1
20020091392 Michelson Jul 2002 A1
20020116009 Fraser et al. Aug 2002 A1
20020123753 Michelson Sep 2002 A1
20020128715 Bryan et al. Sep 2002 A1
20020165550 Frey et al. Nov 2002 A1
20020177897 Michelson Nov 2002 A1
20020198532 Michelson Dec 2002 A1
20030009224 Kuras Jan 2003 A1
20030023245 Ralph et al. Jan 2003 A1
20030028249 Baccelli et al. Feb 2003 A1
20030040746 Mitchell et al. Feb 2003 A1
20030045884 Robie et al. Mar 2003 A1
20030045939 Casutt Mar 2003 A1
20030074076 Ferree et al. Apr 2003 A1
20030083747 Winterbottom et al. May 2003 A1
20030100951 Serhan et al. May 2003 A1
20030125739 Bagga et al. Jul 2003 A1
20030130662 Michelson Jul 2003 A1
20030135277 Bryan et al. Jul 2003 A1
20030139812 Garcia et al. Jul 2003 A1
20030187448 Michelson Oct 2003 A1
20030191536 Ferree Oct 2003 A1
20030195517 Michelson Oct 2003 A1
20030195631 Ferree Oct 2003 A1
20030199982 Bryan Oct 2003 A1
20030204261 Eisermann et al. Oct 2003 A1
20030208271 Kuras Nov 2003 A1
20030229358 Errico et al. Dec 2003 A1
20030233145 Landry et al. Dec 2003 A1
20030233155 Slemmer et al. Dec 2003 A1
20030236520 Lim et al. Dec 2003 A1
20040002761 Rogers et al. Jan 2004 A1
20040024407 Ralph et al. Feb 2004 A1
20040024410 Olson et al. Feb 2004 A1
20040030391 Ferree Feb 2004 A1
20040034426 Errico et al. Feb 2004 A1
20040054411 Kelly et al. Mar 2004 A1
20040059318 Zhang et al. Mar 2004 A1
20040073307 Keller Apr 2004 A1
20040073311 Ferree Apr 2004 A1
20040073312 Eisermann et al. Apr 2004 A1
20040093087 Ferree et al. May 2004 A1
20040097928 Zdeblick et al. May 2004 A1
20040098131 Bryan et al. May 2004 A1
20040117021 Biedermann et al. Jun 2004 A1
20040143270 Zucherman et al. Jul 2004 A1
20040143332 Krueger et al. Jul 2004 A1
20040143334 Ferree Jul 2004 A1
20040167626 Geremakis et al. Aug 2004 A1
20040176843 Zubok et al. Sep 2004 A1
20040186569 Berry Sep 2004 A1
20040215342 Suddaby Oct 2004 A1
20040225295 Zubok et al. Nov 2004 A1
20040225365 Eisermann et al. Nov 2004 A1
20040236426 Ralph et al. Nov 2004 A1
20040254644 Taylor Dec 2004 A1
20050015094 Keller Jan 2005 A1
20050015095 Keller Jan 2005 A1
20050015152 Sweeney Jan 2005 A1
20050021145 De et al. Jan 2005 A1
20050021146 De et al. Jan 2005 A1
20050027360 Webb et al. Feb 2005 A1
20050038515 Kunzler Feb 2005 A1
20050043800 Paul et al. Feb 2005 A1
20050085917 Marnay et al. Apr 2005 A1
20050107881 Alleyne et al. May 2005 A1
20050113842 Bertagnoli et al. May 2005 A1
20050113928 Cragg et al. May 2005 A1
20050143824 Richelsoph et al. Jun 2005 A1
20050149189 Mokhtar et al. Jul 2005 A1
20050154463 Trieu Jul 2005 A1
20050165408 Puno et al. Jul 2005 A1
20050192586 Zucherman et al. Sep 2005 A1
20050192670 Zubok et al. Sep 2005 A1
20050197706 Hovorka et al. Sep 2005 A1
20050216081 Taylor et al. Sep 2005 A1
20050216084 Fleischmann et al. Sep 2005 A1
20050234553 Gordon Oct 2005 A1
20050251260 Gerber et al. Nov 2005 A1
20050251261 Peterman Nov 2005 A1
20050261772 Filippi et al. Nov 2005 A1
20050267580 Suddaby Dec 2005 A1
20050267581 Marnay et al. Dec 2005 A1
20060004377 Keller Jan 2006 A1
20060004453 Bartish et al. Jan 2006 A1
20060015183 Gilbert et al. Jan 2006 A1
20060020342 Ferree et al. Jan 2006 A1
20060025862 Villiers et al. Feb 2006 A1
20060029186 De et al. Feb 2006 A1
20060030857 De et al. Feb 2006 A1
20060030862 De et al. Feb 2006 A1
20060036325 Paul et al. Feb 2006 A1
20060041313 Allard et al. Feb 2006 A1
20060041314 Millard Feb 2006 A1
20060052870 Ferree Mar 2006 A1
20060069439 Zucherman et al. Mar 2006 A1
20060142858 Colleran et al. Jun 2006 A1
20060142862 Diaz et al. Jun 2006 A1
20060155378 Eckman Jul 2006 A1
20060167549 Mathys, Jr. et al. Jul 2006 A1
20060178744 De et al. Aug 2006 A1
20060178746 Bartish, Jr. et al. Aug 2006 A1
20060195097 Evans et al. Aug 2006 A1
20060200239 Rothman et al. Sep 2006 A1
20060224241 Butler et al. Oct 2006 A1
20060235426 Lim et al. Oct 2006 A1
20060235525 Gil et al. Oct 2006 A1
20060235527 Buettner-Janz et al. Oct 2006 A1
20060241641 Albans et al. Oct 2006 A1
20060241766 Felton et al. Oct 2006 A1
20060259144 Trieu Nov 2006 A1
20060259146 Navarro et al. Nov 2006 A1
20060265068 Schwab Nov 2006 A1
20060293752 Moumene et al. Dec 2006 A1
20060293754 DeVilliers et al. Dec 2006 A1
20070010826 Rhoda et al. Jan 2007 A1
20070021837 Ashman Jan 2007 A1
20070032875 Blacklock et al. Feb 2007 A1
20070061011 De et al. Mar 2007 A1
20070067035 Falahee Mar 2007 A1
20070067036 Hudgins et al. Mar 2007 A1
20070073398 Fabian et al. Mar 2007 A1
20070093898 Schwab et al. Apr 2007 A1
20070100453 Parsons et al. May 2007 A1
20070100454 Burgess et al. May 2007 A1
20070100456 Dooris et al. May 2007 A1
20070123903 Raymond et al. May 2007 A1
20070123904 Stad et al. May 2007 A1
20070135923 Peterman et al. Jun 2007 A1
20070162133 Doubler et al. Jul 2007 A1
20070168033 Kim et al. Jul 2007 A1
20070168036 Ainsworth et al. Jul 2007 A1
20070179615 Heinz et al. Aug 2007 A1
20070213821 Kwak et al. Sep 2007 A1
20070233077 Khalili Oct 2007 A1
20070233247 Schwab Oct 2007 A1
20070233248 Schwab et al. Oct 2007 A1
20070233251 Abdou Oct 2007 A1
20070233261 Lopez et al. Oct 2007 A1
20070270970 Trieu Nov 2007 A1
20070282449 De et al. Dec 2007 A1
20070299521 Glenn Dec 2007 A1
20080015698 Marino et al. Jan 2008 A1
20080015701 Garcia et al. Jan 2008 A1
20080021557 Trieu Jan 2008 A1
20080051900 De et al. Feb 2008 A1
20080051901 De et al. Feb 2008 A1
20080114453 Francis May 2008 A1
20080125864 De et al. May 2008 A1
20080133011 De et al. Jun 2008 A1
20080133014 Gately et al. Jun 2008 A1
20080154301 De et al. Jun 2008 A1
20080154382 De et al. Jun 2008 A1
20080215155 De et al. Sep 2008 A1
20080228274 De et al. Sep 2008 A1
20080228277 De et al. Sep 2008 A1
20080294259 De et al. Nov 2008 A1
20090043391 De et al. Feb 2009 A1
20090048674 Zubok et al. Feb 2009 A1
20090048677 McLeod et al. Feb 2009 A1
20090076614 Arramon Mar 2009 A1
20090105833 Hovda et al. Apr 2009 A1
20090105834 Hovda et al. Apr 2009 A1
20090105835 Hovda et al. Apr 2009 A1
20090222101 De et al. Sep 2009 A1
20090276051 Arramon et al. Nov 2009 A1
20100004746 Arramon Jan 2010 A1
20100016972 Jansen et al. Jan 2010 A1
20100016973 De et al. Jan 2010 A1
20160242928 Villiers et al. Aug 2016 A1
20160296339 Villiers et al. Oct 2016 A1
Foreign Referenced Citations (55)
Number Date Country
3023353 Apr 1981 DE
0333990 Sep 1989 EP
0333990 May 1990 EP
0560140 Sep 1993 EP
0560141 Sep 1993 EP
0591712 Apr 1994 EP
0820740 Jan 1998 EP
1142544 Oct 2001 EP
1153582 Nov 2001 EP
1153582 Nov 2001 EP
1250898 Oct 2002 EP
1306064 May 2003 EP
1344493 Sep 2003 EP
1344506 Sep 2003 EP
1344507 Sep 2003 EP
1344508 Sep 2003 EP
1405615 Apr 2004 EP
1417940 May 2004 EP
1570813 Sep 2005 EP
2803741 Jul 2001 FR
S61122859 Jun 1986 JP
S63164948 Jul 1988 JP
H01136655 May 1989 JP
06007391 Jan 1994 JP
2002521090 Jul 2002 JP
2003508119 Mar 2003 JP
WO-9920209 Apr 1999 WO
WO-9930651 Jun 1999 WO
WO-0004851 Feb 2000 WO
WO-0035384 Jun 2000 WO
WO-0042954 Jul 2000 WO
WO-0042954 Nov 2000 WO
WO-0101893 Jan 2001 WO
WO-0115637 Mar 2001 WO
WO-0168003 Sep 2001 WO
WO-0211650 Feb 2002 WO
WO-0211650 Sep 2003 WO
WO-2004000170 Dec 2003 WO
WO-2004000171 Dec 2003 WO
WO-2004026187 Apr 2004 WO
WO-2004054477 Jul 2004 WO
WO-2005004756 Jan 2005 WO
WO-2005004756 May 2005 WO
WO-2005053580 Jun 2005 WO
WO-2005072662 Aug 2005 WO
WO-2005112834 Dec 2005 WO
WO-2005112834 May 2006 WO
WO-2006119092 Nov 2006 WO
WO-2006119092 Dec 2006 WO
WO-2007010161 Jan 2007 WO
WO-2007028098 Mar 2007 WO
WO-2007121320 Oct 2007 WO
WO-2007121320 Jun 2008 WO
WO-2010009153 Jan 2010 WO
200603171 Sep 2007 ZA
Non-Patent Literature Citations (17)
Entry
Buttner-Janz, The Development of the Artificial Disc. Introduction, pp. 1-18, Library of Congress Catalogue No. 92-75582, ISBN 0-9635430-0-8 (1989).
Hellier, et al., Wear Studies for Development of an Intervertebral Disc Prosthesis. Spine, vol. 17 No. 6 Supplement pp. 86-96 (1992).
International search report and written opinion dated Oct. 30, 2009 for PCT/US2009/050575.
Lee, et al. Impact Response of the Intervertebral Disc in a Finite-Element Model. Spine. 2000; 25(19):2431-2439.
Lehuec, et al. Shock Absorption in Lumber Disc Prosthesis. Journal of Spinal Disorders & Techniques. 2003; 16(4):346-351.
Notice of allowance dated Feb. 11, 2016 for U.S. Appl. No. 14/467,274.
Notice of allowance dated Aug. 8, 2014 for U.S. Appl. No. 12/504,042.
Office action dated Jan. 20, 2017 for U.S. Appl. No. 15/187,569.
Office action dated Apr. 18, 2014 for U.S. Appl. No. 12/504,042.
“Office action dated May 1, 2017 for U.S. Appl. No. 15/144,689”.
“Office action dated May 4, 2017 for U.S. Appl. No. 15/187,569”.
Office action dated Jul. 24, 2012 for U.S. Appl. No. 12/504,042.
Office action dated Jul. 29, 2013 for U.S. Appl. No. 12/504,042.
Office action dated Sep. 16, 2016 for U.S. Appl. No. 15/144,689.
Office action dated Sep. 16, 2016 for U.S. Appl. No. 15/187,569.
“Office action dated Sep. 18, 2017 for U.S. Appl. No. 15/187,569”.
Office action dated Dec. 18, 2012 for U.S. Appl. No. 12/504,042.
Related Publications (1)
Number Date Country
20200214850 A1 Jul 2020 US
Provisional Applications (1)
Number Date Country
61081952 Jul 2008 US
Divisions (2)
Number Date Country
Parent 14467274 Aug 2014 US
Child 15144689 US
Parent 12504042 Jul 2009 US
Child 14467274 US
Continuations (1)
Number Date Country
Parent 15144689 May 2016 US
Child 16824127 US