WO1996000523A1 - Biopsy needle assembly and guide - Google Patents

Biopsy needle assembly and guide Download PDF

Info

Publication number
WO1996000523A1
WO1996000523A1 PCT/US1995/008126 US9508126W WO9600523A1 WO 1996000523 A1 WO1996000523 A1 WO 1996000523A1 US 9508126 W US9508126 W US 9508126W WO 9600523 A1 WO9600523 A1 WO 9600523A1
Authority
WO
WIPO (PCT)
Prior art keywords
cannula
guide
handle
biopsy
distal end
Prior art date
Application number
PCT/US1995/008126
Other languages
French (fr)
Inventor
Jan Como Rodriguez
Terrence W. Snyder
Original Assignee
Baxter International 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 Baxter International Inc. filed Critical Baxter International Inc.
Priority to AU29511/95A priority Critical patent/AU2951195A/en
Publication of WO1996000523A1 publication Critical patent/WO1996000523A1/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B10/00—Other methods or instruments for diagnosis, e.g. instruments for taking a cell sample, for biopsy, for vaccination diagnosis; Sex determination; Ovulation-period determination; Throat striking implements
    • A61B10/02—Instruments for taking cell samples or for biopsy
    • A61B10/0233—Pointed or sharp biopsy instruments
    • A61B10/025—Pointed or sharp biopsy instruments for taking bone, bone marrow or cartilage samples

Definitions

  • the invention relates generally to the field of medical instruments, and more particularly to those instruments employed in biopsy, aspiration, and transplant procedures of bone marrow. Background of the nvention
  • a "core" of bone marrow it is desirable to retrieve a "core" of bone marrow to examine bone marrow archi ⁇ tecture. This procedure may be useful in determin ⁇ ing whether a patient has cancer and the extent of cancerous cells that may exist. Examining a bone marrow core typically involves an extended period of time in which the core is first prepared and then sliced into thin samples which are examined under a microscope.
  • All bone marrow biopsy, aspiration and transplant needles currently on the market have a handle with a cannula extending outwardly from the handle.
  • the handle is used by the doctor to apply force to the cannula as the cannula punctures the bone.
  • Such needles typically include a stylet with a sharpened tip which is inserted through the cannu- la and is used to initially puncture the bone.
  • the stylet also serves to occlude the cannula while the bone is punctured so that the marrow sample subse ⁇ quently taken is free from bone chips.
  • the stylet is then removed and bone marrow is withdrawn from the patient by manipulating the cannula to cause bone marrow to move into the interior of the cannu ⁇ la.
  • Bone marrow needles have traditionally been designed so that the needle is attached to the cen ⁇ ter of the handle. While many physicians feel com ⁇ fortable with a centrally attached needle, it has now been discovered that it may be easier to guide a needle with a user's index finger when the needle is not centrally located on the handle of the needle assembly. It has also recently been discovered that when an off-center device is used, it is important to insure that a physician's arm, wrist, and index finger are all generally in alignment with the can- nula of the needle to provide enhanced control over the needle. Examples of such devices are described in U.S.
  • the handle has an proximal surface which has a some ⁇ what saddle shaped offset surface which, when grasped by a physician, conforms to the shape of the physician's palm.
  • the off-center radius causes the handle to have a first relatively narrow end and a second relatively wide end.
  • the handle also has a curved, convex, lower surface designed to be easily gripped by a user's fingers.
  • the proximal end of the cannula is con ⁇ nected to the lower surface of the handle toward the relatively narrow end.
  • the cannula handle is connected to the cannula at an oblique angle that places the user's wrist and forearm in general alignment with the user's index finger and the axis of the cannula.
  • the invention provides a guide for a bone biopsy needle assembly that includes an elongated tubular cannula having an axially extend ⁇ ing lumen therethrough.
  • the guide which is provid ⁇ ed to facilitate insertion of a probe into the can ⁇ nula for sample removal, has a molded shape with an elongated dimension having first and second ends.
  • a cylindrical opening extends through the length of the elongated dimension and has a diameter substan ⁇ tially equal to that of the interior lumen of the cannula.
  • a flared outward enlargement of the cylindrical opening at each of the first and second ends provides for easy alignment of one of the ends with the distal end of the cannula and the other end forms a guide for insertion of a probe into the dis ⁇ tal end of the cannula for removal of the biopsy specimen.
  • the guide of this invention is preferably of an hourglass shape. Further aspects of the inven ⁇ tion will be apparent from the detailed description and accompanying drawings. Brief Description of the Drawings
  • Figure 1 is a side elevational view of the biopsy needle assembly of this invention
  • Figure 2 is a perspective view of a biopsy needle assembly of this invention with the stylet withdrawn from the cannula;
  • Figure 3 is a fragmentary perspective view of the cannula handle component of the system with the cover in the open position to expose the proximal cannula assembly;
  • Figure 4 is a fragmentary enlarged view of the cannula tip with parts shown in cross-section;
  • Figure 5 is a side elevational expanded fragmentary view of a stylet tip
  • Figure 6 is a perspective rear view of the cannula handle with cavity cover in the open posi- tion to show the hinge detail;
  • Figure 7 is a fragmentary cross-sectional view of the handle with stylet in place shown in the closed position;
  • Figure 8 is a view of the handle of Figure
  • Figure 9 is a fragmentary cross-sectional view taken along line 9-9 of Figure 8;
  • Figure 10 is a fragmentary perspective view illustrating the manner in which the device of this invention is grasped and illustrating the initial entry into a body;
  • Figure 11 shows a view of the device of Figure 10 as it is penetrating a bone
  • Figure 12 is a view of the device of Figure 10 after the marrow cavity of the bone has been en ⁇ tered and showing the withdrawal of the stylet;
  • Figure 13 shows the device of Figure 10 during aspiration of material utilizing a syringe
  • Figures 14-17 illustrate the use of the de ⁇ vice of Figure 10 to reenter the bone cavity to ob ⁇ tain a biopsy specimen
  • Figure 18 illustrates the use of a probe guide and probe to remove a biopsy specimen from the cannula
  • Figure 19 is a side view of the probe guide and fragmentary cannula tip with parts broken away and in section. Detailed Description of a Preferred Embodiment
  • a biopsy needle assembly 10 which in ⁇ cludes a hollow cannula 12 having an open, sharpened distal end 13, and being attached to a handle 11 at its proximal end.
  • Handle 11 is provided with a cov- er 16 that pivots open to the position seen in Fig ⁇ ures 2 and 3 to expose a gap or hollow portion 19 of the handle into which the cannula hub 30, which is secured to the proximal end of cannula 12, is open.
  • Ends 15 and 17 of handle 14 extend laterally and have central axes that are attached to cannula 12 at an oblique angle with respect to the cannula axis so as to form a saddle shaped configuration that will conform to the hand of a user.
  • End 15 which is de- signed to be grasped by the forefinger and thumb of the user is of a smaller cross-section and shorter than end 17 which is designed to engage the user's palm.
  • Handle 11 is formed from a bottom portion 14, which includes cover 16 which is hinged to the bottom portion 14.
  • Upper lateral end portions of the handle 15 and 17 are preferably formed from a single molded piece connected together by means of a flat connecting portion 21 that forms a bottom to hollow portion 19 of the handle assembly.
  • the han ⁇ dle can, thus, conveniently be formed from two mold ⁇ ed parts.
  • a hollow tubular cannula hub 30 is molded to the proximal end of cannula 12 and serves to se ⁇ cure the cannula 12 to handle 11 by tight frictional engagement of hub 30 in an aperture through the dis ⁇ tal surface of bottom 14 of the handle 11. Hub 30 extends upwardly into hollow portion 19.
  • cannula hub 30 is connected in fluid flow communication with the hollow interior of can- nula 12 as can best be seen in Figures 7 and 8.
  • Can ⁇ nula hub 30, as well as any other parts coming into fluid contact, are preferably formed from a polysty ⁇ rene terpolymer of acrylonitrile, butadiene and sty- rene (ABS) or, alternatively, a polycarbonate poly- mer.
  • a stylet having a shaft 22 and a handle 24 fits within the handle 11 with the distal end 26 of the stylet extending beyond the distal end 13 of cannula 12.
  • Knob 24 is provided with a proximal projection 25 in order to provide additional com ⁇ pression resistance to the knob and to provide a surface against which internal ribs 40 of the handle are supported during use of the instrument.
  • Cover portion 16 is hingedly connected to the bottom part 14 of handle 11 by means of living hinges 34, 36 and 38.
  • living hinges 34, 36 and 38 In the preferred configura ⁇ tion of these hinges best seen in Figures 6 and 8, it will be noted that the outermost hinges 34 and 36 are pivoted at a higher point on the base portion 14 of the handle than is the inner hinge 38.
  • the upper end of central living hinge 38 is also hinged nearer the perimeter of cover 16. This causes rota ⁇ tional pivoting of cover 16 as it is opened, causing it to pivot out of the way of knob 14 more rapidly than would otherwise be the case.
  • This hinge ar ⁇ rangement also holds the cover in a relatively ele ⁇ vated position as seen in Figure 8 when open.
  • the handle components 14, 15, 16 and 17 are all preferably provided with ribs 40 to provide structural integrity and light weight to the handle 11. These components are all preferably formed from a polyolefin such as a high density polyethylene, polypropylene, or a polyester or similar thermoplas ⁇ tic polymeric material.
  • the cover 16 is preferably provided with end walls 42 that provide a chamber surrounding knob 24 when the cover is in the closed position. Walls 42 thus provide a degree of resis ⁇ tance to rotation of the knob 24, preventing rela ⁇ tive rotation between stylet 22 and cannula 12.
  • the base portion 21 is provided with up- wardly extending projections 44 and 48.
  • Knob 24 also fits tightly over the outside of projections 48, thus forming a structure that prevents relative rotation of stylet 22 and cannula 12 even when substantial force is applied to the needle assembly by the physician.
  • Lip 54 of cover 16 fits within the bottom part of handle 14 as can be seen in Figure 7.
  • An indentation 58 is provided in lower handle portion 14 to matingly receive a projection 56 of the cover in order to retain the cover in a closed position.
  • a ridge 60 is provided to form a surface to be grasped in order to open cover 16.
  • FIG. 10-19 The procedure for use of the instrument of this invention is shown in Figures 10-19.
  • the needle grasped in physician's hand 70, is introduced through an incision, through soft tissue 72 toward and into contact with bone structure 74, usually the posterior iliac crest.
  • the needle is advanced into the marrow cavity by alternating 45 clockwise/counter-clockwise rotation.
  • the cover 16 is then opened as seen in Figure 12 and the stylet removed from the cannula.
  • Sample aspiration syringe 76 is then attached to the can ⁇ nula hub 30, which is preferably provided with a luer fitting for that purpose. Negative pressure is applied by quickly withdrawing the syringe plunger to remove an aspirated specimen.
  • the biopsy procedure is illustrated in Fig ⁇ ures 15-19, wherein another penetration to the mar ⁇ row cavity is made, and after removal of the stylet, the cannula is advanced into the marrow cavity to obtain a specimen.
  • a knob (not shown) similar to the stylet knob 24 is included with the needle assembly and is placed in the handle to fill the space provided for knob 24.
  • the specimen is de ⁇ tached from surrounding tissue by redirection and rotation of the cannula a number of times in each direction.
  • the specimen is removed from the cannula as shown in Figure 19 by introducing a probe 82 through the distal end of the cannula utilizing the probe guide 80 to insure easy insertion of the probe into the lumen of the cannula.
  • the biopsy specimen is then pushed up into the proximal end of the can ⁇ nula and through the cannula hub.
  • probe guide 80 is preferably a molded plastic shape in the form of a generally hourglass configuration.
  • a cylindrical opening 81 extends through the length of said elon ⁇ gated dimension of the guide between its ends.
  • the cylindrical elongated opening has a diameter sub ⁇ stantially equal to that of said interior lumen of cannula 12.

Abstract

A bone biopsy needle assembly (10) includes an elongated tubular cannula (12) having an axially extending lumen therethrough. A guide (80) is provided to facilitate insertion of a probe into the cannula (12) for sample removal. The guide (80) has a molded shape with an elongated dimension and flared cylindrical openings.

Description

BIOPSY NEEDLE ASSEMBLY AND GUIDE Technical Field
The invention relates generally to the field of medical instruments, and more particularly to those instruments employed in biopsy, aspiration, and transplant procedures of bone marrow. Background of the nvention
It is frequently desirable to take biopsy samples from a patient. In bone marrow biopsy, it is always necessary to puncture the bone of a pa¬ tient in order to retrieve bone marrow which normal¬ ly exists only in the center of a bone.
It may be desirable to retrieve bone marrow for several different reasons. In one type of bone marrow procedure, it is desirable to retrieve a "core" of bone marrow to examine bone marrow archi¬ tecture. This procedure may be useful in determin¬ ing whether a patient has cancer and the extent of cancerous cells that may exist. Examining a bone marrow core typically involves an extended period of time in which the core is first prepared and then sliced into thin samples which are examined under a microscope.
In other bone marrow procedures, it is desirable to simply aspirate a portion of the bone marrow to make a relatively rapid examination to indicate the state of a patient's disease and to aid in the diagnosis of a patient.
Finally, in other bone marrow procedures, multiple aspirations of bone marrow are conducted to perform a bone marrow transplant. While each of these procedures has different goals, they all re¬ quire that the bone be punctured in order to access the bone marrow within. Thus, it is important to provide a needle which enhances the ability of the user to puncture bone with minimal trauma to the patient.
All bone marrow biopsy, aspiration and transplant needles currently on the market have a handle with a cannula extending outwardly from the handle. The handle is used by the doctor to apply force to the cannula as the cannula punctures the bone. Such needles typically include a stylet with a sharpened tip which is inserted through the cannu- la and is used to initially puncture the bone. The stylet also serves to occlude the cannula while the bone is punctured so that the marrow sample subse¬ quently taken is free from bone chips. The stylet is then removed and bone marrow is withdrawn from the patient by manipulating the cannula to cause bone marrow to move into the interior of the cannu¬ la. In some cases a slight suction is applied to the cannula to hold the bone marrow in place as the cannula is removed from the patient. Bone marrow needles have traditionally been designed so that the needle is attached to the cen¬ ter of the handle. While many physicians feel com¬ fortable with a centrally attached needle, it has now been discovered that it may be easier to guide a needle with a user's index finger when the needle is not centrally located on the handle of the needle assembly. It has also recently been discovered that when an off-center device is used, it is important to insure that a physician's arm, wrist, and index finger are all generally in alignment with the can- nula of the needle to provide enhanced control over the needle. Examples of such devices are described in U.S. Patents 4,469,109 and 4,838,282. Objects of the Invention It is an object of the invention to provide a bone marrow needle assembly having a guide for assistance in inserting a probe into the cannula tip for removal therefrom of a biopsy specimen.
It is still another object of the invention to provide a bone marrow needle assembly with a guide having a shape suited for ease of handling and placement over the distal end of a cannula to facil¬ itate alignment of the guide and, subsequently, a specimen removal probe, with the cannula. Summary of the Invention
In a preferred embodiment of the invention the handle has an proximal surface which has a some¬ what saddle shaped offset surface which, when grasped by a physician, conforms to the shape of the physician's palm. The off-center radius causes the handle to have a first relatively narrow end and a second relatively wide end. The handle also has a curved, convex, lower surface designed to be easily gripped by a user's fingers. In the preferred e - bodiment, the proximal end of the cannula is con¬ nected to the lower surface of the handle toward the relatively narrow end. Thus, when a user grips the handle, the user's index finger can be naturally applied to the cannula to guide the cannula into a patient. The cannula handle is connected to the cannula at an oblique angle that places the user's wrist and forearm in general alignment with the user's index finger and the axis of the cannula.
Briefly, the invention provides a guide for a bone biopsy needle assembly that includes an elongated tubular cannula having an axially extend¬ ing lumen therethrough. The guide, which is provid¬ ed to facilitate insertion of a probe into the can¬ nula for sample removal, has a molded shape with an elongated dimension having first and second ends. A cylindrical opening extends through the length of the elongated dimension and has a diameter substan¬ tially equal to that of the interior lumen of the cannula. A flared outward enlargement of the cylindrical opening at each of the first and second ends provides for easy alignment of one of the ends with the distal end of the cannula and the other end forms a guide for insertion of a probe into the dis¬ tal end of the cannula for removal of the biopsy specimen.
The guide of this invention is preferably of an hourglass shape. Further aspects of the inven¬ tion will be apparent from the detailed description and accompanying drawings. Brief Description of the Drawings
Figure 1 is a side elevational view of the biopsy needle assembly of this invention;
Figure 2 is a perspective view of a biopsy needle assembly of this invention with the stylet withdrawn from the cannula;
Figure 3 is a fragmentary perspective view of the cannula handle component of the system with the cover in the open position to expose the proximal cannula assembly; Figure 4 is a fragmentary enlarged view of the cannula tip with parts shown in cross-section;
Figure 5 is a side elevational expanded fragmentary view of a stylet tip;
Figure 6 is a perspective rear view of the cannula handle with cavity cover in the open posi- tion to show the hinge detail;
Figure 7 is a fragmentary cross-sectional view of the handle with stylet in place shown in the closed position; Figure 8 is a view of the handle of Figure
7 with the cover shown in the open position and with the stylet partially withdrawn from the cannula;
Figure 9 is a fragmentary cross-sectional view taken along line 9-9 of Figure 8; Figure 10 is a fragmentary perspective view illustrating the manner in which the device of this invention is grasped and illustrating the initial entry into a body;
Figure 11 shows a view of the device of Figure 10 as it is penetrating a bone;
Figure 12 is a view of the device of Figure 10 after the marrow cavity of the bone has been en¬ tered and showing the withdrawal of the stylet;
Figure 13 shows the device of Figure 10 during aspiration of material utilizing a syringe;
Figures 14-17 illustrate the use of the de¬ vice of Figure 10 to reenter the bone cavity to ob¬ tain a biopsy specimen;
Figure 18 illustrates the use of a probe guide and probe to remove a biopsy specimen from the cannula; and
Figure 19 is a side view of the probe guide and fragmentary cannula tip with parts broken away and in section. Detailed Description of a Preferred Embodiment
Referring more particularly to the drawings there is seen a biopsy needle assembly 10 which in¬ cludes a hollow cannula 12 having an open, sharpened distal end 13, and being attached to a handle 11 at its proximal end. Handle 11 is provided with a cov- er 16 that pivots open to the position seen in Fig¬ ures 2 and 3 to expose a gap or hollow portion 19 of the handle into which the cannula hub 30, which is secured to the proximal end of cannula 12, is open. Ends 15 and 17 of handle 14 extend laterally and have central axes that are attached to cannula 12 at an oblique angle with respect to the cannula axis so as to form a saddle shaped configuration that will conform to the hand of a user. End 15 which is de- signed to be grasped by the forefinger and thumb of the user is of a smaller cross-section and shorter than end 17 which is designed to engage the user's palm.
Handle 11 is formed from a bottom portion 14, which includes cover 16 which is hinged to the bottom portion 14. Upper lateral end portions of the handle 15 and 17 are preferably formed from a single molded piece connected together by means of a flat connecting portion 21 that forms a bottom to hollow portion 19 of the handle assembly. The han¬ dle can, thus, conveniently be formed from two mold¬ ed parts. A hollow tubular cannula hub 30 is molded to the proximal end of cannula 12 and serves to se¬ cure the cannula 12 to handle 11 by tight frictional engagement of hub 30 in an aperture through the dis¬ tal surface of bottom 14 of the handle 11. Hub 30 extends upwardly into hollow portion 19. The hollow interior of cannula hub 30 is connected in fluid flow communication with the hollow interior of can- nula 12 as can best be seen in Figures 7 and 8. Can¬ nula hub 30, as well as any other parts coming into fluid contact, are preferably formed from a polysty¬ rene terpolymer of acrylonitrile, butadiene and sty- rene (ABS) or, alternatively, a polycarbonate poly- mer. A stylet having a shaft 22 and a handle 24 fits within the handle 11 with the distal end 26 of the stylet extending beyond the distal end 13 of cannula 12. Knob 24 is provided with a proximal projection 25 in order to provide additional com¬ pression resistance to the knob and to provide a surface against which internal ribs 40 of the handle are supported during use of the instrument.
Cover portion 16 is hingedly connected to the bottom part 14 of handle 11 by means of living hinges 34, 36 and 38. In the preferred configura¬ tion of these hinges best seen in Figures 6 and 8, it will be noted that the outermost hinges 34 and 36 are pivoted at a higher point on the base portion 14 of the handle than is the inner hinge 38. The upper end of central living hinge 38 is also hinged nearer the perimeter of cover 16. This causes rota¬ tional pivoting of cover 16 as it is opened, causing it to pivot out of the way of knob 14 more rapidly than would otherwise be the case. This hinge ar¬ rangement also holds the cover in a relatively ele¬ vated position as seen in Figure 8 when open.
The handle components 14, 15, 16 and 17 are all preferably provided with ribs 40 to provide structural integrity and light weight to the handle 11. These components are all preferably formed from a polyolefin such as a high density polyethylene, polypropylene, or a polyester or similar thermoplas¬ tic polymeric material. The cover 16 is preferably provided with end walls 42 that provide a chamber surrounding knob 24 when the cover is in the closed position. Walls 42 thus provide a degree of resis¬ tance to rotation of the knob 24, preventing rela¬ tive rotation between stylet 22 and cannula 12. The base portion 21 is provided with up- wardly extending projections 44 and 48. Projections 44 on the forward and rearward sides of the handle closely engage curved indentations 46 in the lower part of knob 24. Knob 24 also fits tightly over the outside of projections 48, thus forming a structure that prevents relative rotation of stylet 22 and cannula 12 even when substantial force is applied to the needle assembly by the physician.
Lip 54 of cover 16 fits within the bottom part of handle 14 as can be seen in Figure 7. An indentation 58 is provided in lower handle portion 14 to matingly receive a projection 56 of the cover in order to retain the cover in a closed position. A ridge 60 is provided to form a surface to be grasped in order to open cover 16.
The procedure for use of the instrument of this invention is shown in Figures 10-19. As seen in Figure 10, the needle, grasped in physician's hand 70, is introduced through an incision, through soft tissue 72 toward and into contact with bone structure 74, usually the posterior iliac crest. The needle is advanced into the marrow cavity by alternating 45 clockwise/counter-clockwise rotation. The cover 16 is then opened as seen in Figure 12 and the stylet removed from the cannula. For sample aspiration syringe 76 is then attached to the can¬ nula hub 30, which is preferably provided with a luer fitting for that purpose. Negative pressure is applied by quickly withdrawing the syringe plunger to remove an aspirated specimen.
The biopsy procedure is illustrated in Fig¬ ures 15-19, wherein another penetration to the mar¬ row cavity is made, and after removal of the stylet, the cannula is advanced into the marrow cavity to obtain a specimen. Optionally, a knob (not shown) similar to the stylet knob 24 is included with the needle assembly and is placed in the handle to fill the space provided for knob 24. The specimen is de¬ tached from surrounding tissue by redirection and rotation of the cannula a number of times in each direction. The specimen is removed from the cannula as shown in Figure 19 by introducing a probe 82 through the distal end of the cannula utilizing the probe guide 80 to insure easy insertion of the probe into the lumen of the cannula. The biopsy specimen is then pushed up into the proximal end of the can¬ nula and through the cannula hub.
As best seen in Figure 20, probe guide 80 is preferably a molded plastic shape in the form of a generally hourglass configuration. A cylindrical opening 81 extends through the length of said elon¬ gated dimension of the guide between its ends. The cylindrical elongated opening has a diameter sub¬ stantially equal to that of said interior lumen of cannula 12. Preferably there is at each end of the opening a flared outward enlargement 84 for align¬ ment with the distal end of the cannula and for forming a guide for insertion of probe 82 into said distal end of the cannula for removal of a biopsy specimen.

Claims

What is claimed is;
1. A guide for removal of a biopsy specimen from the interior of a cannula having a hollow cylindrical interior lumen for recovery of biopsy specimens and having an open distal end co - prising: a molded shape having an elongated dimen¬ sion with first and second ends, a cylindrical opening extending through the length of said elongated dimension between said first and second ends, said elongated opening having a diameter substantially equal to that of said interior lumen of said cannula, and a flared outward enlargement of said cylindrical opening at each of said first and second ends for alignment of one of said first and second ends with said distal end of said cannula and the other of said first and second distal ends forming a guide for insertion of a probe into said distal end of said cannula for removal of said biopsy spec¬ imen.
2. A guide according to claim 1 wherein said molded shape is in the form of a generally hourglass configuration.
3. A guide according to claim 1 formed of a molded polymeric material.
PCT/US1995/008126 1994-06-29 1995-06-28 Biopsy needle assembly and guide WO1996000523A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU29511/95A AU2951195A (en) 1994-06-29 1995-06-28 Biopsy needle assembly and guide

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US26823094A 1994-06-29 1994-06-29
US08/268,230 1994-06-29

Publications (1)

Publication Number Publication Date
WO1996000523A1 true WO1996000523A1 (en) 1996-01-11

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AU (1) AU2951195A (en)
WO (1) WO1996000523A1 (en)

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US5476102A (en) 1995-12-19

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