EP1596777A2 - Instruments and methods for aligning implants for insertion - Google Patents

Instruments and methods for aligning implants for insertion

Info

Publication number
EP1596777A2
EP1596777A2 EP04710719A EP04710719A EP1596777A2 EP 1596777 A2 EP1596777 A2 EP 1596777A2 EP 04710719 A EP04710719 A EP 04710719A EP 04710719 A EP04710719 A EP 04710719A EP 1596777 A2 EP1596777 A2 EP 1596777A2
Authority
EP
European Patent Office
Prior art keywords
clamp assembly
instrument
alignment instrument
assembly
alignment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04710719A
Other languages
German (de)
French (fr)
Inventor
Lukas Eisermann
Tai Friesem
Jean-Charles Lehuec
Matthews Hallet
Jeffrey Zhang
Thomas Zdeblick
Loic Josse
Liu Mingyan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Warsaw Orthopedic Inc
Original Assignee
SDGI Holdings Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SDGI Holdings Inc filed Critical SDGI Holdings Inc
Priority claimed from PCT/US2004/004534 external-priority patent/WO2004071360A2/en
Publication of EP1596777A2 publication Critical patent/EP1596777A2/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/16Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
    • A61B17/1642Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans for producing a curved bore
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/16Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
    • A61B17/1662Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans for particular parts of the body
    • A61B17/1671Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans for particular parts of the body for the spine
    • AHUMAN NECESSITIES
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    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/16Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
    • A61B17/17Guides or aligning means for drills, mills, pins or wires
    • A61B17/1739Guides or aligning means for drills, mills, pins or wires specially adapted for particular parts of the body
    • A61B17/1757Guides or aligning means for drills, mills, pins or wires specially adapted for particular parts of the body for the spine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/44Joints for the spine, e.g. vertebrae, spinal discs
    • A61F2/4455Joints for the spine, e.g. vertebrae, spinal discs for the fusion of spinal bodies, e.g. intervertebral fusion of adjacent spinal bodies, e.g. fusion cages
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    • A61B17/16Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
    • A61B17/1613Component parts
    • A61B17/1622Drill handpieces
    • A61B17/1624Drive mechanisms therefor
    • AHUMAN NECESSITIES
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    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/84Fasteners therefor or fasteners being internal fixation devices
    • A61B17/86Pins or screws or threaded wires; nuts therefor
    • AHUMAN NECESSITIES
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    • A61F2/4603Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
    • A61F2/4611Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof of spinal prostheses
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    • A61F2/02Prostheses implantable into the body
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    • A61F2002/2835Bone graft implants for filling a bony defect or an endoprosthesis cavity, e.g. by synthetic material or biological material
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30003Material related properties of the prosthesis or of a coating on the prosthesis
    • A61F2002/3006Properties of materials and coating materials
    • A61F2002/3008Properties of materials and coating materials radio-opaque, e.g. radio-opaque markers
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/3011Cross-sections or two-dimensional shapes
    • A61F2002/30159Concave polygonal shapes
    • A61F2002/30166H-shaped or I-shaped
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30362Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit with possibility of relative movement between the protrusion and the recess
    • A61F2002/3037Translation along the common longitudinal axis, e.g. piston
    • A61F2002/30373Translation along the common longitudinal axis, e.g. piston with additional means for preventing said translation
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    • A61F2002/30383Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by laterally inserting a protrusion, e.g. a rib into a complementarily-shaped groove
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    • A61F2/02Prostheses implantable into the body
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    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surface, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • A61F2002/30899Protrusions pierced with apertures
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surface, e.g. coating for improving bone ingrowth
    • A61F2002/30925Special external or bone-contacting surface, e.g. coating for improving bone ingrowth etched
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2220/00Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2220/0025Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2220/0033Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementary-shaped recess, e.g. held by friction fit
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0002Two-dimensional shapes, e.g. cross-sections
    • A61F2230/0028Shapes in the form of latin or greek characters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2250/00Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2250/0058Additional features; Implant or prostheses properties not otherwise provided for
    • A61F2250/0096Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers
    • A61F2250/0098Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers radio-opaque, e.g. radio-opaque markers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00017Iron- or Fe-based alloys, e.g. stainless steel
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00023Titanium or titanium-based alloys, e.g. Ti-Ni alloys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00005The prosthesis being constructed from a particular material
    • A61F2310/00011Metals or alloys
    • A61F2310/00029Cobalt-based alloys, e.g. Co-Cr alloys or Vitallium
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2310/00Prostheses classified in A61F2/28 or A61F2/30 - A61F2/44 being constructed from or coated with a particular material
    • A61F2310/00389The prosthesis being coated or covered with a particular material
    • A61F2310/00592Coating or prosthesis-covering structure made of ceramics or of ceramic-like compounds
    • A61F2310/00796Coating or prosthesis-covering structure made of a phosphorus-containing compound, e.g. hydroxy(l)apatite

Definitions

  • the present disclosure relates generally to the field of orthopedics and spinal surgery, and in some embodiments, the present disclosure relates to instrumentation and methods for the insertion of prosthetic devices.
  • Implantation of prosthetic devices and associated tools and instrumentation has heretofore been accomplished with the aid of complex electronic equipment such as intraoperative X-ray (Fluoroscopy) equipment.
  • complex electronic equipment such as intraoperative X-ray (Fluoroscopy) equipment.
  • the use of such equipment can bear burdensome costs while the complexity of the equipment complicates the procedures associated with the use of the equipment.
  • Alternatives to the use of complex electronic equipment during the insertion of prosthetic devices into the human body are therefore desirable.
  • the instrument includes an annular housing, a plunger member disposed within the annular housing and adapted to be moved therethrough, and an anchoring device partially disposed within the annular housing, the anchoring device adapted to be driven by the plunger member.
  • An assembly for aligning a prosthetic device for insertion into an intervertebral space includes means for anchoring an alignment instrument in a vertebral body disposed adjacent to the intervertebral space, means for operatively connecting an implantation device to the alignment instrument, the prosthetic device being disposed on the implantation device, and means for adjusting the implantation device to position the prosthetic device adjacent to the intervertebral space.
  • the assembly includes an alignment instrument, a first clamp assembly slidably engaged with the alignment instrument, a second clamp assembly slidably engaged with the first clamp assembly, and an implantation device slidably engaged with the second clamp assembly, the implantation device being adapted to retain a prosthetic device thereon.
  • a method for aligning a prosthetic device for insertion into an intervertebral space includes providing an alignment instrument having an anchoring device extending therefrom, engaging the anchoring device with a vertebral body located adjacent to the intervertebral space, aligning the alignment instrument relative to the intervertebral space, driving the anchoring device into the vertebral body, and providing an implantation device adjacent to the alignment instrument via a clamp assembly operatively connected to the alignment instrument, the implantation device holding the prosthetic device at a distal end thereof.
  • Fig. 1 is an anterior view of an intervertebral space defined between a pair of vertebral bodies.
  • Fig. 2 is a perspective view of an assembly incorporating an alignment instrument and an implantation device according to one embodiment of the present disclosure.
  • Fig. 3 A is a sectional view of the alignment instrument of Fig. 2.
  • Fig. 3B is a detailed view of a portion of the alignment instrument of Fig. 3 A.
  • Fig. 4 is a perspective view of the assembly of Fig. 2 shown schematically in use during implantation of a prosthetic device.
  • Fig. 5 is an exploded view of an alternative alignment instrument according to another embodiment of the present disclosure.
  • This disclosure relates generally to instrumentation and methods for delivering prosthetic devices under mechanical guidance and, in some instances, providing limited fluoroscopic guidance to aid in such mechanical guidance.
  • FIG. 1 shown therein is an anterior view of a portion of a spinal column 10, illustrating a pair of adjacent upper and lower vertebrae Nl and N2 separated by an intervertebral space S created by the removal of a natural intervertebral disc.
  • the illustration of two vertebrae is only intended as an example. Another example would be a sacrum and one vertebrae.
  • an assembly for aiding in the implantation of a prosthetic device into the intervertebral space S (Fig. 1) is generally referred to by reference numeral 20, and is shown, in one embodiment, as including an alignment instrument 22 and an associated implantation device 24. It is understood that the alignment instrument 22 may be used to aid in the implantation of a variety of prosthetic devices such as screws, cages, total joint implants, etc. In one embodiment, the alignment instrument 22 is generally linear in shape and extends along an X-axis defined by the longitudinal axis of the alignment instrument.
  • the alignment instrument 22 includes a plunger member 26 positioned within a generally annular housing 28 of the instrument, and a knob 30 integrally formed with the proximal end of the plunger member 26. In this manner, rotation of the knob 30 is adapted to impart rotation to the plunger member 26.
  • An anchoring device such as a threaded bone screw 32, is disposed within the distal end of the alignment instrument 22 to receive a rotational and a translational force from the plunger member 26 as will be further described.
  • the bone screw 32 is formed of a radiopaque material such as steel.
  • proximal refers to the direction generally towards a user, such as a surgeon (not shown), of the alignment instrument 20, and the term “distal” refers to the direction generally towards a patient (not shown).
  • an inner annular surface 34 of the housing 28 includes a threaded portion 36 for receiving and engaging a corresponding threaded portion 38 of the plunger member 26. Accordingly, rotation of the plunger member 26 via the knob 30, not only rotates the plunger member in the housing, but translates the plunger member through the housing 24 as well.
  • the distal end of the plunger member 26 includes a spherical-shaped groove 40 formed therein, which is adapted to engage a spherical head 42 of the bone screw 32.
  • the distal end of the housing 28 is reduced in diameter and chamfered to allow a threaded portion 44 of the bone screw 32 to rotate relative to the housing, while retaining the head 42 of the bone screw within the housing.
  • the alignment instrument 22 is also configured to provide radiographic alignment, and as such, the proximal portion of the alignment instrument is increased in diameter relative to the distal portion of the alignment instrument to house a radiographic marker generally depicted by reference numeral 46.
  • the radiographic marker 46 includes a pair of rings 48, 50.
  • the ring 48 is positioned within the proximal portion of the alignment instrument 22 and, accordingly, has a diameter corresponding to fit within the diameter of the proximal portion.
  • the ring 50 is positioned within the distal portion of the alignment instrument 20 and, accordingly, has a diameter corresponding to fit within the diameter of the distal portion.
  • the rings 48, 50 cooperate to aid with alignment as will be described.
  • the rings 48, 50 may be formed of any radiographic material such as metal.
  • the rings 48, 50 may be replaced with alternative radiographic markers such as metal rods configured to form an X-like shape, thereby also aiding in alignment.
  • a pair of clamp assemblies 52, 54 are provided to operatively connect the alignment instrument 22 with the associated implantation device 24.
  • the implantation device 24 is substantially similar to the instrument described in U.S. Patent Application Serial No. 10/430,473, which is herein incorporated by reference for all legitimate purposes.
  • the inner clamp assembly 52 (relative to the alignment instrument 22) is adapted to slidably engage the alignment instrument 22, and as such, includes a groove 56 defined through an adjustable clamping portion 57 to facilitate the slidable engagement.
  • the inner clamp assembly 52 includes a connector 58, which is adapted to releasably secure the inner clamp assembly 52 to the alignment instrument 22.
  • the connector 58 is threaded through the inner clamp assembly 52 to contact the clamping portion 57, and thus can be actuated to engage or disengage the clamping portion with the alignment instrument 22. Accordingly, the inner clamp assembly 52 is adjustable along the X-axis defined by the alignment instrument 22, yet can be secured to the alignment instrument upon adjustment of the inner clamp assembly 52 to a desired position.
  • the outer clamp assembly 54 (relative to the alignment instrument 22) is adapted to slidably engage the inner clamp assembly 52.
  • the outer clamp assembly 54 includes a groove 60 defined therein for allowing the outer clamp assembly to slidably engage the inner clamp assembly 52 via a flange portion 62 of the inner clamp assembly.
  • the outer clamp assembly 54 is adjustable relative to the inner clamp assembly 52 along a Y-axis.
  • the outer clamp assembly 54 is laterally adjustable relative to the alignment instrument 22.
  • the outer clamp assembly 54 further includes a connector 64, which is adapted to releasably secure the outer clamp assembly 54 to the inner clamp assembly 52.
  • the connector 64 is threaded through the outer clamp assembly 54, and thus can be actuated to engage or disengage with the inner clamp assembly 52.
  • the inner clamp assembly 52 is rotatable about the alignment instrument 22. Therefore, although described as being a lateral axis as viewed in Fig. 2, descriptions of the Y-axis can change depending on the position of the inner clamp assembly 52 relative to the alignment instrument 22. For example, the inner clamp assembly 52 can be rotated to position the implantation device 24 in the same horizontal plane as the alignment instrument 22. In this example, the outer clamp assembly 54 is still adjustable along the Y- axis, but the Y-axis would be considered an elevational axis.
  • the outer clamp assembly 54 is further adapted to receive the implantation device 24 (Fig. 4) via a pair of grooves 66, 68 formed in a pair of corresponding clamping portions 70, 72, respectively, of the outer clamp assembly.
  • the implantation device 24 is adapted for placement within the grooves 66, 68 such that the implantation device is slidable relative to the outer clamp assembly 54.
  • an additional connector 74 is associated with the outer clamp assembly 54 to advance the clamping portion 70 towards the clamping portion 72, thereby securing the implantation device 24 within the outer clamp assembly 52 upon adjustment of the implantation device to a desired position.
  • the connector 74 is adjustable along a threaded rod (not shown) associated with the clamping portion 70, and thus, the clamping portion 70 can be actuated towards the clamping portion 72 via adjustment of the connector 74.
  • the implantation device 24 is adjustable along an A-axis defined by the longitudinal axis of the implantation device.
  • the implantation device 24 can be rotated within the outer clamp assembly 54 to adjust to correspond to different positions of the outer clamp assembly relative to the inner clamp assembly 52, and as such, the implantation device is rotatable about the A-axis.
  • the bone screw 32 is adapted to be inserted into the vertebrae Nl to provide an anchor point from which to align the associated implantation device 24 prior to insertion of a prosthetic device, generally depicted by reference numeral 80, into the intervertebral space S.
  • a prosthetic device generally depicted by reference numeral 80
  • the bone screw 32 may alternatively be inserted into the vertebrae N2.
  • a fluoroscopic machine, or C-arm 82 is further provided to f ⁇ uoroscopically aid in positioning of the alignment instrument 22.
  • the alignment instrument 22 is aligned with fluoroscopic assistance by positioning the C-arm 82 in a direct anterior view of the vertebrae Nl, N2 for corresponding to an anterior/oblique insertion approach.
  • the alignment instrument 22 is then positioned such that the bone screw 32 engages the upper vertebra Nl.
  • the bone screw 32 is positioned relatively close to a midline of the upper vertebra Nl, however, it is understood that the exact position of the bone screw relative to the upper vertebra is not critical.
  • the plunger member 26 (Figs. 3A, 3B) is driven against the bone screw 32 to drive the bone screw into the upper vertebra Nl, thereby providing a fixed anchor location defined by the position of the bone screw.
  • the proximal portion of the alignment instrument 22 is then adjusted to align the radiographic marker 46 with the spherical head 42 of the bone screw 32 as viewed on a monitor (not shown) associated with the C-arm 82. Upon proper alignment determined by viewing the monitor, the alignment instrument 22 is then locked into place by further advancement of the plunger member 26 against the bone screw 32.
  • the implantation device 24 is then placed within the grooves 66, 68 of the outer clamp assembly 54. The position of the implantation device 24 is then adjusted to correspond to the center of the intervertebral space S, and upon reaching the desired position, the position of the implantation device is locked by engaging the connector 64 against the inner clamp assembly 52.
  • the implantation device 24 is further adjustable along the A-axis to properly position the prosthetic device 80 for implantation into the intervertebral space S.
  • proper positioning entails positioning the prosthetic device 80 proximate to the vertebral bodies Nl, N2 to the point of touching.
  • the implantation device 24 is locked along the A-axis by engaging the connector 74 against the outer clamp assembly 54. The implantation device 24 is then actuated to insert the prosthetic device 80 into the intervertebral space S.
  • alignment instrument 90 includes a bubble level device 92, which in one embodiment, eliminates the need for radiographic markers and a C- arm fluoroscopic machine.
  • the alignment instrument 90 is substantially similar to the alignment instrument 22 except for the features described below, and, as such, features of the alignment instrument 90 that are substantially similar to features of the alignment instrument 22 are given the same reference numerals.
  • the alignment instrument 90 includes a substantially uniform housing 94 through which the plunger member 26 is adapted to move through to engage the bone screw 32.
  • the alignment instrument 90 is adapted for use with the bubble level 92, which may connect with the alignment instrument 90 in any conventional manner, such as via a threaded connection.
  • the bubble level 92 may include a threaded connector 96 for engaging a threaded receptacle 98 defined in the alignment instrument 90.
  • the bubble level 92 may be integrally formed with the alignment instrument 90.
  • the bubble level 92 is conventional in most respects, and therefore, includes a cavity (not shown) defined therethrough for holding fluid, and a transparent portion 100 for viewing the fluid.
  • the alignment instrument 90 is used in conjunction with the inner and outer clamp assemblies 52, 54 to align the prosthetic device 80 for insertion into the intervertebral space S.
  • the patient Prior to anchoring of the alignment instrument 90, the patient (not shown) is first aligned at a substantially 90° angle relative to the operating table (not shown).
  • the bone screw 32 of the alignment instrument 90 is then inserted into the upper vertebra Nl to provide an anchoring point.
  • the proximal, or free, end of the alignment instrument 90 is then aligned to the proper position by adjusting the alignment instrument 90 until the bubble level 92 reflects a neutral position.
  • a probe may be used in conjunction with the alignment instrument 22, 90 prior to placement of the implantation device 24.
  • a probe may be used in conjunction with the alignment instrument 22, 90 prior to placement of the implantation device 24.
  • proper alignment of the various instrumentation relative to the intervertebral space S may be further ensured.
  • the anchoring device is described as a bone screw, a variety of anchoring devices may be used with the alignment instruments 22, 90.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biomedical Technology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Surgery (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Dentistry (AREA)
  • Neurology (AREA)
  • Cardiology (AREA)
  • Transplantation (AREA)
  • Vascular Medicine (AREA)
  • Prostheses (AREA)

Abstract

A fusion-promoting, spinal plating assembly is described. The plating assembly includes a first plate, and at least one additional plate connected to the first plate, the at least one additional plate extending transversely to the first plate. The plating assembly is adapted to be completely inserted within an intervertebral space defined between a first vertebral body and a second vertebral body.

Description

INSTRUMENTS AND METHODS FOR ALIGNING IMPLANTS FOR INSERTION
Cross-Reference to Related Applications
This application claims the benefit of U.S. Provisional Application No. 60/446,963 filed on February 12, 2003. U.S. Provisional Application No. 60/446,963 is herein incorporated by reference for all legitimate purposes. This application is also related to U.S. Patent Application Serial No. 10/430,473, which is herein incorporated by reference for all legitimate purposes.
Background
The present disclosure relates generally to the field of orthopedics and spinal surgery, and in some embodiments, the present disclosure relates to instrumentation and methods for the insertion of prosthetic devices.
In the treatment of diseases, injuries or malformations affecting spinal motion segments, and especially those affecting disc tissue, it has long been known to remove some or all of a degenerated, ruptured or otherwise failing disc. In cases involving intervertebral disc tissue that has been removed or is otherwise absent from a spinal motion segment, corrective measures are taken to ensure the proper spacing of the vertebrae formerly separated by the removed disc tissue. In some instances, prosthetic devices are inserted into the disc space to maintain the structural integrity of the spinal column.
Implantation of prosthetic devices and associated tools and instrumentation has heretofore been accomplished with the aid of complex electronic equipment such as intraoperative X-ray (Fluoroscopy) equipment. However, the use of such equipment can bear burdensome costs while the complexity of the equipment complicates the procedures associated with the use of the equipment. Alternatives to the use of complex electronic equipment during the insertion of prosthetic devices into the human body are therefore desirable.
Therefore, what is needed is are instrumentation and methods for aligning implants for insertion, which reduce, or eliminate, the use of fluoroscopic equipment. Summary
An instrument for aiding in aligning a prosthetic device for insertion into an intervertebral space is described. The instrument includes an annular housing, a plunger member disposed within the annular housing and adapted to be moved therethrough, and an anchoring device partially disposed within the annular housing, the anchoring device adapted to be driven by the plunger member.
An assembly for aligning a prosthetic device for insertion into an intervertebral space is provided. The assembly includes means for anchoring an alignment instrument in a vertebral body disposed adjacent to the intervertebral space, means for operatively connecting an implantation device to the alignment instrument, the prosthetic device being disposed on the implantation device, and means for adjusting the implantation device to position the prosthetic device adjacent to the intervertebral space.
An assembly for aligning a prosthetic device for insertion into an intervertebral space is provided. The assembly includes an alignment instrument, a first clamp assembly slidably engaged with the alignment instrument, a second clamp assembly slidably engaged with the first clamp assembly, and an implantation device slidably engaged with the second clamp assembly, the implantation device being adapted to retain a prosthetic device thereon.
A method for aligning a prosthetic device for insertion into an intervertebral space is described. The method includes providing an alignment instrument having an anchoring device extending therefrom, engaging the anchoring device with a vertebral body located adjacent to the intervertebral space, aligning the alignment instrument relative to the intervertebral space, driving the anchoring device into the vertebral body, and providing an implantation device adjacent to the alignment instrument via a clamp assembly operatively connected to the alignment instrument, the implantation device holding the prosthetic device at a distal end thereof.
Brief Description of the Drawings
Fig. 1 is an anterior view of an intervertebral space defined between a pair of vertebral bodies.
Fig. 2 is a perspective view of an assembly incorporating an alignment instrument and an implantation device according to one embodiment of the present disclosure.
Fig. 3 A is a sectional view of the alignment instrument of Fig. 2. Fig. 3B is a detailed view of a portion of the alignment instrument of Fig. 3 A.
Fig. 4 is a perspective view of the assembly of Fig. 2 shown schematically in use during implantation of a prosthetic device.
Fig. 5 is an exploded view of an alternative alignment instrument according to another embodiment of the present disclosure.
Description
This disclosure relates generally to instrumentation and methods for delivering prosthetic devices under mechanical guidance and, in some instances, providing limited fluoroscopic guidance to aid in such mechanical guidance. For the purposes of promoting an understanding of the principles of the disclosure, reference will now be made to the embodiments, or examples, illustrated in the drawings and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the disclosure is thereby intended. Any alterations and further modifications in the described embodiments, and any further applications of the principles of the disclosure as described herein are contemplated as would normally occur to one skilled in the art to which this disclosure relates. As such, individual features of separately described embodiments can be combined to form additional embodiments.
Referring now to Fig. 1, shown therein is an anterior view of a portion of a spinal column 10, illustrating a pair of adjacent upper and lower vertebrae Nl and N2 separated by an intervertebral space S created by the removal of a natural intervertebral disc. The illustration of two vertebrae is only intended as an example. Another example would be a sacrum and one vertebrae.
Referring now to Figs. 2, 3 A and 3B, an assembly for aiding in the implantation of a prosthetic device into the intervertebral space S (Fig. 1) is generally referred to by reference numeral 20, and is shown, in one embodiment, as including an alignment instrument 22 and an associated implantation device 24. It is understood that the alignment instrument 22 may be used to aid in the implantation of a variety of prosthetic devices such as screws, cages, total joint implants, etc. In one embodiment, the alignment instrument 22 is generally linear in shape and extends along an X-axis defined by the longitudinal axis of the alignment instrument. The alignment instrument 22 includes a plunger member 26 positioned within a generally annular housing 28 of the instrument, and a knob 30 integrally formed with the proximal end of the plunger member 26. In this manner, rotation of the knob 30 is adapted to impart rotation to the plunger member 26. An anchoring device, such as a threaded bone screw 32, is disposed within the distal end of the alignment instrument 22 to receive a rotational and a translational force from the plunger member 26 as will be further described. In one embodiment, the bone screw 32 is formed of a radiopaque material such as steel. In the present disclosure, the term "proximal" refers to the direction generally towards a user, such as a surgeon (not shown), of the alignment instrument 20, and the term "distal" refers to the direction generally towards a patient (not shown).
In one embodiment, an inner annular surface 34 of the housing 28 includes a threaded portion 36 for receiving and engaging a corresponding threaded portion 38 of the plunger member 26. Accordingly, rotation of the plunger member 26 via the knob 30, not only rotates the plunger member in the housing, but translates the plunger member through the housing 24 as well. As better seen in Fig. 3B, the distal end of the plunger member 26 includes a spherical-shaped groove 40 formed therein, which is adapted to engage a spherical head 42 of the bone screw 32. In the present example, the distal end of the housing 28 is reduced in diameter and chamfered to allow a threaded portion 44 of the bone screw 32 to rotate relative to the housing, while retaining the head 42 of the bone screw within the housing.
The alignment instrument 22 is also configured to provide radiographic alignment, and as such, the proximal portion of the alignment instrument is increased in diameter relative to the distal portion of the alignment instrument to house a radiographic marker generally depicted by reference numeral 46. In one embodiment, the radiographic marker 46 includes a pair of rings 48, 50. The ring 48 is positioned within the proximal portion of the alignment instrument 22 and, accordingly, has a diameter corresponding to fit within the diameter of the proximal portion. The ring 50 is positioned within the distal portion of the alignment instrument 20 and, accordingly, has a diameter corresponding to fit within the diameter of the distal portion. As such, the rings 48, 50 cooperate to aid with alignment as will be described. It is understood that the rings 48, 50 may be formed of any radiographic material such as metal. It is further understood that the rings 48, 50 may be replaced with alternative radiographic markers such as metal rods configured to form an X-like shape, thereby also aiding in alignment.
Referring again to Fig. 2, a pair of clamp assemblies 52, 54 are provided to operatively connect the alignment instrument 22 with the associated implantation device 24. In one embodiment, the implantation device 24 is substantially similar to the instrument described in U.S. Patent Application Serial No. 10/430,473, which is herein incorporated by reference for all legitimate purposes. The inner clamp assembly 52 (relative to the alignment instrument 22) is adapted to slidably engage the alignment instrument 22, and as such, includes a groove 56 defined through an adjustable clamping portion 57 to facilitate the slidable engagement. The inner clamp assembly 52 includes a connector 58, which is adapted to releasably secure the inner clamp assembly 52 to the alignment instrument 22. In the present example, the connector 58 is threaded through the inner clamp assembly 52 to contact the clamping portion 57, and thus can be actuated to engage or disengage the clamping portion with the alignment instrument 22. Accordingly, the inner clamp assembly 52 is adjustable along the X-axis defined by the alignment instrument 22, yet can be secured to the alignment instrument upon adjustment of the inner clamp assembly 52 to a desired position.
The outer clamp assembly 54 (relative to the alignment instrument 22) is adapted to slidably engage the inner clamp assembly 52. In one embodiment, the outer clamp assembly 54 includes a groove 60 defined therein for allowing the outer clamp assembly to slidably engage the inner clamp assembly 52 via a flange portion 62 of the inner clamp assembly. Accordingly, the outer clamp assembly 54 is adjustable relative to the inner clamp assembly 52 along a Y-axis. For example, in the embodiment of Fig. 2, the outer clamp assembly 54 is laterally adjustable relative to the alignment instrument 22. The outer clamp assembly 54 further includes a connector 64, which is adapted to releasably secure the outer clamp assembly 54 to the inner clamp assembly 52. In the present example, the connector 64 is threaded through the outer clamp assembly 54, and thus can be actuated to engage or disengage with the inner clamp assembly 52.
As can be appreciated, the inner clamp assembly 52 is rotatable about the alignment instrument 22. Therefore, although described as being a lateral axis as viewed in Fig. 2, descriptions of the Y-axis can change depending on the position of the inner clamp assembly 52 relative to the alignment instrument 22. For example, the inner clamp assembly 52 can be rotated to position the implantation device 24 in the same horizontal plane as the alignment instrument 22. In this example, the outer clamp assembly 54 is still adjustable along the Y- axis, but the Y-axis would be considered an elevational axis.
The outer clamp assembly 54 is further adapted to receive the implantation device 24 (Fig. 4) via a pair of grooves 66, 68 formed in a pair of corresponding clamping portions 70, 72, respectively, of the outer clamp assembly. The implantation device 24 is adapted for placement within the grooves 66, 68 such that the implantation device is slidable relative to the outer clamp assembly 54. Moreover, an additional connector 74 is associated with the outer clamp assembly 54 to advance the clamping portion 70 towards the clamping portion 72, thereby securing the implantation device 24 within the outer clamp assembly 52 upon adjustment of the implantation device to a desired position. In the present example, the connector 74 is adjustable along a threaded rod (not shown) associated with the clamping portion 70, and thus, the clamping portion 70 can be actuated towards the clamping portion 72 via adjustment of the connector 74. As such, the implantation device 24 is adjustable along an A-axis defined by the longitudinal axis of the implantation device. Of course, the implantation device 24 can be rotated within the outer clamp assembly 54 to adjust to correspond to different positions of the outer clamp assembly relative to the inner clamp assembly 52, and as such, the implantation device is rotatable about the A-axis.
Referring to Fig. 4, in one embodiment, the bone screw 32 is adapted to be inserted into the vertebrae Nl to provide an anchor point from which to align the associated implantation device 24 prior to insertion of a prosthetic device, generally depicted by reference numeral 80, into the intervertebral space S. Of course, the bone screw 32 may alternatively be inserted into the vertebrae N2. A fluoroscopic machine, or C-arm 82, is further provided to fϊuoroscopically aid in positioning of the alignment instrument 22. For sake of clarity, the method for aligning the alignment instrument 22 for insertion of the prosthetic device 80 will be described with respect to the anterior/oblique approach to the intervertebral space S; however, it is understood that the alignment process, in a general sense, is adaptable for other approaches to the interverterbral space including the lateral approach. In operation, and with continued reference to Fig. 4, the alignment instrument 22 is aligned with fluoroscopic assistance by positioning the C-arm 82 in a direct anterior view of the vertebrae Nl, N2 for corresponding to an anterior/oblique insertion approach. The alignment instrument 22 is then positioned such that the bone screw 32 engages the upper vertebra Nl. In one embodiment, the bone screw 32 is positioned relatively close to a midline of the upper vertebra Nl, however, it is understood that the exact position of the bone screw relative to the upper vertebra is not critical. Upon proper positioning, the plunger member 26 (Figs. 3A, 3B) is driven against the bone screw 32 to drive the bone screw into the upper vertebra Nl, thereby providing a fixed anchor location defined by the position of the bone screw.
The proximal portion of the alignment instrument 22 is then adjusted to align the radiographic marker 46 with the spherical head 42 of the bone screw 32 as viewed on a monitor (not shown) associated with the C-arm 82. Upon proper alignment determined by viewing the monitor, the alignment instrument 22 is then locked into place by further advancement of the plunger member 26 against the bone screw 32. The implantation device 24 is then placed within the grooves 66, 68 of the outer clamp assembly 54. The position of the implantation device 24 is then adjusted to correspond to the center of the intervertebral space S, and upon reaching the desired position, the position of the implantation device is locked by engaging the connector 64 against the inner clamp assembly 52.
The implantation device 24 is further adjustable along the A-axis to properly position the prosthetic device 80 for implantation into the intervertebral space S. In one embodiment, proper positioning entails positioning the prosthetic device 80 proximate to the vertebral bodies Nl, N2 to the point of touching. Upon proper positioning, the implantation device 24 is locked along the A-axis by engaging the connector 74 against the outer clamp assembly 54. The implantation device 24 is then actuated to insert the prosthetic device 80 into the intervertebral space S.
Thus, the above-described process and associated instrumentation allows for alignment and implantation of the prosthetic device 80 with minimal fluoroscopic guidance. Referring now to Fig. 5, in an alternative embodiment, alignment and insertion of the prosthetic device 80 can be accomplished without fluoroscopic guidance through the use of an alternative alignment instrument 90. The alignment instrument 90 includes a bubble level device 92, which in one embodiment, eliminates the need for radiographic markers and a C- arm fluoroscopic machine. The alignment instrument 90 is substantially similar to the alignment instrument 22 except for the features described below, and, as such, features of the alignment instrument 90 that are substantially similar to features of the alignment instrument 22 are given the same reference numerals.
The alignment instrument 90 includes a substantially uniform housing 94 through which the plunger member 26 is adapted to move through to engage the bone screw 32. The alignment instrument 90 is adapted for use with the bubble level 92, which may connect with the alignment instrument 90 in any conventional manner, such as via a threaded connection. For example, the bubble level 92 may include a threaded connector 96 for engaging a threaded receptacle 98 defined in the alignment instrument 90. Of course, in some embodiments, the bubble level 92 may be integrally formed with the alignment instrument 90. The bubble level 92 is conventional in most respects, and therefore, includes a cavity (not shown) defined therethrough for holding fluid, and a transparent portion 100 for viewing the fluid.
In operation, the alignment instrument 90 is used in conjunction with the inner and outer clamp assemblies 52, 54 to align the prosthetic device 80 for insertion into the intervertebral space S. Prior to anchoring of the alignment instrument 90, the patient (not shown) is first aligned at a substantially 90° angle relative to the operating table (not shown). Upon proper alignment of the patient, the bone screw 32 of the alignment instrument 90 is then inserted into the upper vertebra Nl to provide an anchoring point. The proximal, or free, end of the alignment instrument 90 is then aligned to the proper position by adjusting the alignment instrument 90 until the bubble level 92 reflects a neutral position.
The present disclosure has been described relative to several preferred embodiments. Improvements or modifications that become apparent to persons of ordinary skill in the art after reading this disclosure are deemed within the spirit and scope of the application. For example, during the alignment process, a probe may be used in conjunction with the alignment instrument 22, 90 prior to placement of the implantation device 24. In this manner, proper alignment of the various instrumentation relative to the intervertebral space S may be further ensured. Moreover, although described with reference to an anterior-oblique approach, it is understood that the above-described methods and instrumentation may be used with a variety of insertion approaches. Still further, although the anchoring device is described as a bone screw, a variety of anchoring devices may be used with the alignment instruments 22, 90.
Accordingly, it is understood that several modifications, changes and substitutions are intended in the foregoing disclosure and, in some instances, some features of the disclosure will be employed without a corresponding use of other features. It is also understood that all spatial references, such as "inner," "outer," "proximal," and "distal" are for illustrative purposes only and can be varied within the scope of the disclosure. Accordingly, it is appropriate that the appended claims be construed broadly and in a manner consistent with the scope of the disclosure.

Claims

What is claimed is:
1. An instrument for aiding in aligning a prosthetic device for insertion into an intervertebral space, comprising an annular housing, a plunger member disposed within the annular housing and adapted to be moved therethrough, and an anchoring device partially disposed within the annular housing, the anchoring device adapted to be driven by the plunger member.
2. The instrument of claim 1 wherein the annular housing includes a threaded surface and the plunger member includes a threaded surface for engaging the threaded surface of the annular housing.
3. The instrument of claim 1 wherein the anchoring device is a bone screw.
4. The instrument of claim 1 wherein the annular housing is stepped in diameter to divide the annular housing into a first portion and a second portion, the first portion having a diameter greater than the second portion.
5. The instrument of claim 4 wherein the first portion includes a first radiographic marker housed therein, and the second portion includes a second radiographic marker housed therein, the second radiographic marker having a diameter smaller than that of the first radiographic marker.
6. The instrument of claim 5 wherein the first and second radiographic markers cooperate with a fluoroscopic machine to align the instrument.
7. The instrument of claim 3 wherein the bone screw comprises a spherical- shaped screw head disposed within the annular housing and a threaded connector extending from the screw head to an area outside of the annular housing.
8. The instrument of claim 7 wherein a distal end of the plunger member comprises a recess defined therein, the recess being shaped to correspond to the shape of the screw head.
9. The instrument of claim 1 further comprising a knob operatively connected to the plunger member such that rotation of the knob imparts rotation to the plunger member.
10. The instrument of claim 1 further comprising a bubble level operatively connected to the annular housing.
11. An assembly for aligning a prosthetic device for insertion into an intervertebral space, comprising means for anchoring an alignment instrument in a vertebral body disposed adjacent to the intervertebral space, means for operatively connecting an implantation device to the alignment instrument, the prosthetic device being disposed on the implantation device, and means for adjusting the implantation device to position the prosthetic device adjacent to the intervertebral space.
12. An assembly for aligning a prosthetic device for insertion into an intervertebral space, comprising an alignment instrument, a first clamp assembly slidably engaged with the alignment instrument, a second clamp assembly slidably engaged with the first clamp assembly, and an implantation device slidably engaged with the second clamp assembly, the implantation device being adapted to retain a prosthetic device thereon.
13. The assembly of claim 12 wherein the alignment instrument comprises a means for engaging an anchoring device partially disposed within the alignment instrument and driving the anchoring device into bone.
14. The assembly of claim 13 wherein the alignment instrument further comprises means for aligning the alignment instrument.
15. The assembly of claim 14 wherein the means for aligning the alignment instrument is a radiographic marker adapted to cooperate with a fluoroscopic machine.
16. The assembly of claim 14 wherein the means for aligning the alignment instrument is a bubble level device operatively connected to the alignment instrument.
17. The assembly of claim 12 wherein the first clamp assembly comprises a connector, the connector being adapted to lock the first clamp assembly, thereby restricting movement of the first clamp assembly along the alignment instrument.
18. The assembly of claim 12 wherein the second clamp assembly comprises a connector, the connector being adapted to lock the second clamp assembly, thereby restricting movement of the second clamp assembly along the first clamp assembly.
19. The assembly of claim 18 wherein the second clamp assembly comprises an additional connector, the additional connector being adapted to lock the implantation device, thereby restricting movement of the implantation device along the second clamp assembly.
20. A method for aligning a prosthetic device for insertion into an intervertebral space, comprising providing an alignment instrument having an anchoring device extending therefrom, engaging the anchoring device with a vertebral body located adjacent to the intervertebral space, aligning the alignment instrument relative to the intervertebral space, driving the anchoring device into the vertebral body, and providing an implantation device adjacent to the alignment instrument via a clamp assembly operatively connected to the alignment instrument, the implantation device holding the prosthetic device at a distal end thereof.
21. The method of claim 20 wherein aligning the alignment instrument comprises aligning a radiographic marker disposed within the alignment instrument via a fluoroscopic machine.
22. The method of claim 20 wherein aligning the alignment instrument comprises viewing a bubble level device operatively connected to the alignment instrument.
23. The method of claim 20 wherein the clamp assembly is operatively connected to the alignment instrument via a second clamp assembly.
24. The method of claim 23 further comprising slidably adjusting the second clamp assembly along the alignment instrument to position the prosthetic device adjacent to the intervertebral space
25. The method of claim 24 further comprising locking the second clamp assembly to the alignment instrument.
26. The method of claim 25 further comprising slidably adjusting the first clamp assembly along the second clamp assembly to further position the prosthetic device adjacent to the intervertebral space.
27. The method of claim 26 further comprising locking the first clamp assembly to the second clamp assembly.
28. The method of claim 27 further comprising slidably adjusting the implantation device along the first clamp assembly to further position the prosthetic device adjacent to the intervertebral space.
29. The method of claim 28 further comprising locking the implantation device to the first clamp assembly.
EP04710719A 2003-02-12 2004-02-12 Instruments and methods for aligning implants for insertion Withdrawn EP1596777A2 (en)

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US44696303P 2003-02-12 2003-02-12
US446963P 2003-02-12
US43047303A 2003-05-06 2003-05-06
US430473 2003-05-06
PCT/US2004/004534 WO2004071360A2 (en) 2003-02-12 2004-02-12 Instruments and methods for aligning implants for insertion

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EP04710719A Withdrawn EP1596777A2 (en) 2003-02-12 2004-02-12 Instruments and methods for aligning implants for insertion

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AT (1) ATE505156T1 (en)
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CA2515646A1 (en) 2004-08-26
EP1596772B1 (en) 2011-04-13
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WO2004071346A2 (en) 2004-08-26
AU2004211984A1 (en) 2004-08-26
JP2006517456A (en) 2006-07-27
WO2004071346A3 (en) 2004-10-21
AU2004212017A1 (en) 2004-08-26
JP2006517460A (en) 2006-07-27
EP1596772A2 (en) 2005-11-23
ATE505156T1 (en) 2011-04-15
CA2515767A1 (en) 2004-08-26

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