Implantable medical device delivery system with a frangible portion and methods of making the same

0001This invention generally relates to interventional medical device systems that are navigable through body vessels of a human subject. More particularly, this invention relates to delivery systems for deploying an implantable medical device to a target location of a body vessel and methods of manufacturing the same.

0002The use of catheter delivery systems for positioning and deploying therapeutic devices, such as dilation balloons, stents and embolic coils, in the vasculature of the human body has become a standard procedure for treating endovascular diseases. It has been found that such devices are particularly useful in treating areas where traditional operational procedures are impossible or pose a great risk to the patient, for example in the treatment of aneurysms in cranial blood vessels. Due to the delicate tissue surrounding cranial blood vessels, especially for example brain tissue, it is very difficult and often risky to perform surgical procedures to treat defects of the cranial blood vessels. Advancements in catheter deployment systems have provided an alternative treatment in such cases. Some of the advantages of catheter delivery systems are that they provide methods for treating blood vessels by an approach that has been found to reduce the risk of trauma to the surrounding tissue, and they also allow for treatment of blood vessels that in the past would have been considered inoperable.

0003Typically, these procedures involve inserting the distal end of a delivery catheter into the vasculature of a patient and guiding it through the vasculature to a predetermined delivery location. A vascular occlusion device, such as an embolic coil, is attached to the end of a delivery member which pushes the coil through the catheter and out of the distal end of the catheter into the delivery location. Some of the problems that have been associated with these procedures relate to the accuracy of coil placement. For example, the coil detachment mechanism may cause the embolic coil to partially or fully dislodge from the predetermined location or dislodge previously deployed coils.

0004In response to accuracy concerns, numerous devices and release mechanisms have been developed in an attempt to provide a deployment system which allows control of the occlusion device after the device has been delivered by the catheter and to also provide a rapid release or detachment mechanism to release the device once it is in place. One such detachment system is disclosed in <patcit id="pcit0001" dnum="US5108407A"><text>Geremia et al. U.S. Patent No. 5,108,407</text></patcit>, which shows a fiber optic cable including a connector device mounted to the end to the optic fiber. An embolic coil is attached to the connector device by a heat releasable adhesive. Laser light is transmitted through the fiber optic cable to increase the temperature of the connector device, which melts the adhesive and releases the embolic coil. One drawback to using this type of system is the potential risk of melted adhesives contaminating the blood stream.

0005Another coil deployment system employs a pusher member having an embolic coil attached to the pusher member by a connector fiber which is capable of being broken by heat, as disclosed in <patcit id="pcit0002" dnum="US6478773B"><text>Gandhi et al. U.S. Patent No. 6,478,773</text></patcit>. The pusher member of this arrangement includes an electrical resistance heating coil through which the connector fiber is passed. Electrical current is supplied to the heating coil by a power source connected to the heating coil via wires extending through an internal lumen of the pusher. The power source is activated to increase the temperature of the heating coil which breaks the connector fiber. One drawback is that connecting the resistance heating coil to the power source requires running multiple wires through the pusher member. Additionally, the electrical current traveling through the wires may create stray electromagnetic fields that have the potential to interfere with other surgical and monitoring equipment.

0006Yet another embolic coil positioning and delivery system is described in <patcit id="pcit0003" dnum="US5989242A"><text>Saadat et al. U.S. Patent No. 5,989,242</text></patcit>, which discloses a catheter having a shape memory alloy connector attached to the distal end of the catheter. The connector includes a socket having a pair of spaced-apart fingers which are responsive to a change in temperature. The fingers are bent towards each other and hold a ball which is connected to an end of an embolic coil. The connector absorbs laser light transmitted through an optical cable and transforms the light into heat energy. The heat energy raises the temperature of the connector and opens the fingers, thereby releasing the embolic coil. This type of ball and socket connection is rigid and causes the catheter to be stiff, making it difficult to guide the catheter through the vasculature of the body.

0007The above-identified delivery systems typically require electronic equipment powered by a power source and if the electronic equipment is defective or the power source fails, the procedure may be prolonged while the equipment is repaired or replaced. Prolonging the procedure may expose the patient to additional risk.

0008To avoid the problems associated with such heat- and/or electricity-based detachment systems, numerous mechanical deployment systems have been proposed. For example, <patcit id="pcit0004" dnum="US5250071A"><text>U.S. Patent No. 5,250,071 to Palermo </text></patcit>describes a detachment system whereby interlocking clasps of the system and the coil are held together by a control wire. The control wire is moved proximally to disengage the clasps from each other.

0009While this and similar delivery and detachment systems avoid the need for electronic equipment, many require a separate handle component, such as an attachable handle, a peelable sheath system, and/or a syringe, which is manipulated by the medical professional to release the implantable device. Attachable handle components often require the use of additional components, such as a re-zip sheath, for proper operation with a system including a catheter or introducer component. This tends to increase the time and complexity of releasing the implantable device, as well as increasing the component and packaging costs.

0010Mechanical delivery and detachment systems avoiding the need for an attachable handle and a re-zip sheath are described in <patcit id="pcit0005" dnum="US461231A"><text>U.S. Patent Application Serial Nos. 11/461,231</text></patcit> and <patcit id="pcit0006" dnum="US11461245B"><text>11/461,245 to Mitelberg et al., filed July 31, 2006</text></patcit>. Delivery and detachment systems of <patcit id="pcit0007" dnum="US461245A"><text>U.S. Patent Application Serial No. 11/461,245</text></patcit> are provided with a hypotube having a distal end and a locking member associated with the distal end. The hypotube also has a proximal end separated from the distal end by a spiral-cut portion. The spiral-cut portion is axially movable from a compressed condition to an elongated condition. In one embodiment, the locking member is a wire adapted to engage an implantable medical device when the spiral-cut portion is in the compressed condition. The wire is anchored to the proximal portion of the hypotube, such that movement of the spiral-cut portion from the compressed condition to the elongated condition retracts the wire and causes it to separate from the implantable device, thereby deploying the device to a target location of a body vessel.

0011Delivery and detachment systems according to <patcit id="pcit0008" dnum="US461231A"><text>U.S. Patent Application Serial No. 11/461,231</text></patcit> employ a variation of the deployment system of <patcit id="pcit0009" dnum="US461245A"><text>U.S. Patent Application Serial No. 11/461,245</text></patcit>. In such systems, selected turns of the spiral-cut portion of the hypotube are joined to adjacent turns by frangible bridge members. As the spiral-cut portion is elongated, the bridge members must be broken to fully elongate the spiral-cut portion and retract the locking wire.

0012The delivery and detachment systems of <patcit id="pcit0010" dnum="US461231A"><text>U.S. Patent Application Serial Nos. 11/461,231</text></patcit> and <patcit id="pcit0011" dnum="US11461245B"><text>11/461,245</text></patcit> overcome the above-referenced problems of other known systems, but require the creation of a spiral-cut portion, typically by a laser-cutting operation, during manufacture. Implementation of a spiral-cut portion may increase the difficulty and/or duration of the manufacturing process, so there remains the need for an implantable medical device delivery system incorporating a simplified detachment system.

0013In accordance with one embodiment or aspect of the present invention, a delivery system for delivering an implantable medical device to a target location of a body vessel is provided with a generally hollow tubular carrier member defining a longitudinal axis and having a proximal portion, a distal portion, and a frangible portion intermediate said proximal portion and said distal portion. The frangible portion has at least one notch which provides a break hinge transverse to the longitudinal axis of the carrier member. The frangible portion has a breaking strength about the break hinge which is less than a breaking strength about any other line transverse to the longitudinal axis of the carrier member. The delivery device also includes a locking member at least partially received within the carrier member. The locking member extends at least from the proximal portion of the carrier member to the distal portion of the carrier member and is fixedly secured to the proximal portion. The locking member is adapted to be releasably connected to an implantable medical device.

0014According to another embodiment or aspect of the present invention, a method is provided for manufacturing a delivery system for delivering an implantable medical device to a target location of a body vessel. The method includes providing a generally hollow tubular carrier member having a proximal portion and a distal portion and defining a longitudinal axis. At least one notch is formed in the carrier member intermediate the proximal portion and the distal portion, which notch provides a break hinge transverse to the longitudinal axis. The carrier member has a breaking strength about the break hinge which is less than a breaking strength about any other line transverse to the longitudinal axis. The delivery system is also provided with a locking member at least partially received within the carrier member and extending at least from the proximal portion of the carrier member to the distal portion of the carrier member. A portion of the locking member is fixedly secured to the proximal portion of the carrier member.

0015The delivery system of the present invention may be used in a method is provided for deploying an implantable medical device to a target location of a body vessel. The implantable medical device is positioned generally adjacent to a target location of a body vessel and then the carrier member is broken at the frangible portion along a break hinge transverse to the longitudinal axis. The breaking strength about the break hinge is less than a breaking strength about any other line transverse to the longitudinal axis. The proximal portion of the carrier member is then moved away from the distal portion of the carrier member to retract the locking member, thereby disengaging the locking member from the implantable medical device.

0016Moving the proximal portion of the carrier member away from the distal portion of the carrier member may include moving the proximal portion of the carrier member away from the distal portion of the carrier member along a path substantially parallel to the longitudinal axis of the carrier member.

0017Moving the proximal portion of the carrier member away from the distal portion of the carrier member may include moving the proximal portion of the carrier member away from the distal portion of the carrier member along a path at an angle to the longitudinal axis of the carrier member.

0018The method may further comprise providing an introducer having a lumen and a distal end and positioning said distal end of the introducer generally adjacent to the target location of the body vessel, wherein said positioning the implantable medical device includes moving the implantable medical device through said lumen of the introducer to said distal end of the introducer.

0019The method may further comprise providing an introducer having a lumen and a distal end and positioning at least a portion of the implantable medical device within the lumen at or adjacent to said distal end of the introducer, wherein said positioning the implantable medical device includes positioning the distal end of the introducer and the implantable medical device generally adjacent to the target location of the body vessel.

0020Special application for the present invention has been found for deploying embolic coils to aneurysms in the neurovascular system. However, the present invention is also applicable to the deployment of other devices, including stents, to other portions of the vascular system, so it will be understood that the products and methods described herein are not limited to particular medical devices or particular surgical applications.

0021The present invention will now be described, by way of example only, with reference to the accompanying figures, in which: <ul id="ul0001" list-style="none"><li><figref idref="f0001">Fig. 1</figref> is a side elevational view of a carrier member having a frangible portion with two notches according to an aspect of the present invention;</li><li><figref idref="f0001">Fig. 2</figref> is a top plan view of the carrier member of <figref idref="f0001">Fig. 1</figref>;</li><li><figref idref="f0001">Fig. 3</figref> is a front perspective view of the carrier member of <figref idref="f0001">Fig. 1</figref>;</li><li><figref idref="f0002">Fig. 4</figref> is a partial cross-sectional view of an implantable medical device delivery system incorporating the carrier member of <figref idref="f0001">Fig. 1</figref>;</li><li><figref idref="f0002">Fig. 5</figref> is a partial cross-sectional view of a distal portion of the delivery system of <figref idref="f0002">Fig. 4</figref> in a body vessel;</li><li><figref idref="f0003">Fig. 6</figref> is a partial cross-sectional view of the delivery system of <figref idref="f0002">Fig. 5</figref>, with the frangible portion of the carrier member in a broken condition and the medical device positioned for deployment within an aneurysm;</li><li><figref idref="f0003">Fig. 7</figref> is a cross-sectional view of the frangible portion of a carrier member according to the present invention, taken through the line 7-7 of <figref idref="f0001">Fig. 1</figref>; and</li><li><figref idref="f0004">Fig. 8</figref> is a partial cross-sectional view of the delivery system of <figref idref="f0003">Fig. 6</figref>, with a proximal portion of the carrier member moved away from a distal portion of the carrier member to release the medical device from the delivery system.</li></ul>

0022<figref idref="f0001">Figs. 1-3</figref> illustrate a generally hollow tubular structure or carrier member 10 suitable for incorporation into an implantable medical device delivery system according to an aspect of the present invention. When used herein, the terms "tubular" and "tube" are to be construed broadly and are not limited to a structure that is a right cylinder or strictly circumferential in cross-section or of a uniform cross-section throughout its length. For example, the carrier member 10 is shown as a substantially right cylindrical structure, but may have a tapered or curved outer surface without departing from the scope of the present invention.

0023The carrier member 10 defines a longitudinal axis "A" and has a proximal portion 12, a distal portion 14, and a frangible portion 16 intermediate the proximal portion 12 and the distal portion 14. In one embodiment, the carrier member 10 may be a hypotube comprised of a biocompatible metallic material, such as stainless steel. The hypotube typically will have a diameter of between about 0.203 mm to about 0.508 mm (about 0.008 to about 0.020 inch), at times between about 0.254 mm and 0.381 mm (about 0.010 inch and about 0.015 inch), an example of a specific tube diameter being approximately 0.330 mm (0.013 inch). Such a carrier member is suitable for delivering and deploying embolic coils to target locations, typically aneurysms, within the neurovasculature, but differently sized carrier members comprised of other materials may be useful for different applications and are within the scope of the present invention.

0024The frangible portion 16 comprises at least one open window or notch 18, preferably passing entirely through the wall of the carrier member 10. In the illustrated embodiment of <figref idref="f0001">Figs. 1-3</figref>, the frangible portion 16 comprises two notches 18 which are substantially identical to each other and in facing relationship to each other. Other configurations of the frangible portion 16 are also within the scope of the present invention, such as configurations incorporating a single notch, two or more differently shaped notches, or notches defined by one or more curved walls. The notches 18 weaken the frangible portion 16 compared to the remainder of the carrier member 10, and are useful for deploying an implantable medical device, as will be described in greater detail herein.

0025According to one method of manufacturing the carrier member 10, a generally hollow tubular member and a cutting device (not illustrated) are provided. The nature of the cutting device depends on the material of the tubular member, but a laser is a suitable cutting device for use with a metallic tubular member. In the case of a stainless steel tubular member suitable for use in delivering a neurovascular implant, i.e. a tubular member having an outer diameter no greater than 0.635 mm (0.025 inch), the laser may be adapted to provide a kerf in the range of about 0.127 mm to about 0.381 mm (about 0.005 inch to about 0.015 inch) (a specific example being 0.254 mm (0.010 inch)). The notches 18 are formed by cutting openings into the frangible portion 16.

0026When using a laser, the notches may be formed one or two at a time. To form a single notch, the laser may be applied to the frangible portion along a line generally tangential to the wall of the tubular member. To form two notches in a single carrier member, a pair of tangentially directed lasers may be employed, with each laser separately forming one notch. In yet another embodiment, a single laser may be applied to the frangible portion along a line generally transverse to and through the longitudinal axis of the tubular member. The laser will cut through the wall of the tubular member to define a first notch, pass through the hollow interior, and cut through the wall on the other side of the tubular member to define a second notch in facing relationship to the first notch. If the notch is to be larger than the opening defined by the laser, the laser and/or the tubular member may be moved relative to the other while continuing to operate the laser to fully define the notch.

0027While cutting, and particulary laser-cutting, is one method of forming notches in the carrier member, other methods may be also be employed. For example, the notches may be formed by chemical etching or the like without departing from the scope of the present invention.

0028The delivery system further includes an elongated locking member 20. The locking member 20 may take any of a number of forms including, but not limited to a tube or a wire having a circular or other cross-section. The locking member 20 is at least partially received within the carrier member 10 and fixedly secured to the proximal portion 12. In the embodiment of <figref idref="f0001">Figs. 1-3</figref>, the locking member 20 is illustrated as an actuation wire which is secured to a plug 22 that forms the proximal end of the proximal portion 12. While the locking member 20 is shown as being fixed at the proximal end of the carrier member 10, it may be secured at any area(s) of the proximal portion 12 without departing from the scope of the present invention. The locking member 20 may be comprised of any of a number of materials, typically a metallic material or a polymeric material, and the method of securing the locking member 20 to the proximal portion 12 may vary depending on the material composition of each structure. For example, a number of known methods which may be suitable include, but are not limited to adhesion, welding, soldering, crimping, and swaging.

0029The locking member 20 extends at least from the proximal portion 12 to the distal portion 14 of the carrier member 10. In contrast to the proximal portion 12, the distal portion 14 is not fixedly secured to the locking member 20. Instead, the area of the locking member 20 passing through the distal portion 14 of the carrier member 10 is adapted to be releasably connected to an implantable medical device, such as an embolic coil. As used herein, the phrase "releasably connected" refers to the implantable medical device being temporarily held at or adjacent to the distal portion 14 of the carrier member 10 at least in part by operation of the locking member 20 and being released by manipulation of the locking member 20. Hence, a locking member 20 may be "releasably connected to an implantable medical device" without physically contacting the device, for example, in the case of a locking member that directly engages a detachment mechanism which, in turn, contacts and holds the implantable medical device.

0030In some embodiments, the locking member 20 may extend beyond the distal end of the distal portion 14, which may be advantageous for engagement with an implantable medical device held adjacent to and outside of the distal portion 14 of the carrier member 10, as shown in <figref idref="f0002">Fig. 4</figref> and as will be described in greater detail herein. The locking member 20 may be incorporated into the carrier member 10 before or after the notches 18 are formed, but it may be preferred to apply the notches first to avoid possibly damaging the locking member with a laser or other forming device used to form the notches. [0035] <figref idref="f0002">Fig. 4</figref> shows one embodiment of a fully configured delivery system 24, in partial cross-section and in a pre-deployment condition. In addition to the carrier member 10 and locking member 20, the illustrated delivery system 24 further includes a tubular catheter or introducer 26 and a detachment mechanism generally designated at 28. The introducer 26 may be provided according to known design, sized and configured to be movable through a body vessel and having a lumen adapted to receive at least a portion of the carrier member 10. It will be seen that a carrier member 10 according to the present invention does not require an attachable handle, so it may be used with the introducer 26 without the need for a re-zip sheath. This saves time and reduces complications for physicians and reduces system component costs.

0031The detachment mechanism 28 may take any of a number of configurations, provided that it is adapted to cooperate with the locking member 20 to release an implantable medical device when the locking member 20 is retracted. The illustrated detachment mechanism 28 is associated with the distal portion 14 of the carrier member 10, has an engagement member 30 and a kicker member 32, and conforms generally to the system described in U.S. Patent Application Publication No. <patcit id="pcit0012" dnum="US20070010849A"><text>US 2007/0010849 to Balgobin et al</text></patcit>. The operation of the illustrated detachment mechanism 28 will be described in greater detail herein.

0032The implantable medical device 34 illustrated in <figref idref="f0002">Fig. 4</figref> is an embolic coil. However, it will be appreciated that virtually any implantable medical device may be delivered and deployed by delivery systems according to the present invention.

0033To connect the implantable medical device 34, a portion of the engagement member 30 of the detachment mechanism 28 is passed through an aperture 36 at a proximal end 38 of the implantable medical device 34. Passing the engagement member 30 through the aperture 36 causes the aperture 36 to contact the kicker member 32 and deform the kicker member 32 (which is U-shaped at rest, as shown in <figref idref="f0004">Fig. 8</figref>) to the illustrated condition. The kicker member 32 may be resilient, such that when so deformed it provides a force sufficient to unseat the aperture 36 from the engagement member 30. The implantable medical device 34 is finally locked onto the detachment mechanism 28 by passing a portion of the locking member 20 through an opening of the engagement member 30, as shown in <figref idref="f0002">Fig. 4</figref>. Hence, it will be seen that retracting the locking member 20 will allow the kicker member 32 to return to its original configuration, thereby separating the implantable medical device 34 from the delivery system 24.

0034Regardless of the means employed to secure the implantable medical device 34, a device thus engaged may be delivered to a target location "B" within a body vessel "C" by the introducer 26 (<figref idref="f0002">Fig. 5</figref>). According to one method of delivering the device 34, the introducer 26 is fed through the vasculature until a distal end 40 thereof is adjacent to the target location "B." Thereafter, the distal portion 14 of the carrier member 10 and the associated implantable medical device 34 are advanced through the lumen of the introducer 26 until the device 34 is itself generally adjacent to the target location "B." Alternatively, part of the distal portion 14 of the carrier member 10 and the associated device 34 may be preloaded in the introducer 26, with the combination being fed through the vasculature to the target location "B." Other methods of positioning the implantable medical device 34 generally adjacent to a target location of a body may also be practiced without departing from the scope of the present invention.

0035To more accurately position the engaged device, radiopaque markers (not illustrated) may be attached to the carrier member or the device itself.

0036When the engaged device 34 has been properly positioned and oriented, it is disengaged from the detachment mechanism 28 by retracting the locking member 20. This is initiated by breaking the carrier member 10 at the frangible portion 16, which remains outside of the body of the patient and proximal of the introducer 26, as shown in <figref idref="f0003">Fig. 6</figref>. Preferably, the frangible portion 16 is broken by applying a human digital breaking force generally transverse to the longitudinal axis "A" of the carrier member 10, in the direction of a notch 18 or in the opposite direction. In the embodiment of <figref idref="f0003">Fig. 6</figref>, one notch is facing upwardly and the other is facing downwardly (also shown in <figref idref="f0002">Fig. 4</figref>), so a breaking force may be applied either upwardly or downwardly. <figref idref="f0003">Fig. 6</figref> shows the result of a breaking force applied by holding the distal portion 14 of the carrier member 10 stationary and pressing the proximal portion 12 upwardly such as by grasping same and bending the proximal portion 12 and break the frangible portion 16.

0037A frangible portion 16 with two notches 18 in facing relationship to each other may be an advantageous configuration because it provides a "bi-directional" break hinge "D," as shown in the cross-sectional view of <figref idref="f0003">Fig. 7</figref>. It will be appreciated by those of ordinary skill in that art that the absence of carrier member material at the notches 18 makes them weaker than the remainder of the carrier member 10. When a breaking force is applied according to the foregoing description, the proximal portion 12 bends upwardly about the break hinge "D" until the frangible portion 16 breaks at the notches 18. If a break force is applied to the proximal portion 12 in the opposite direction, the proximal portion 12 will bend downwardly about the break hinge "D" until the frangible portion 16 breaks. When the two notches 18 are substantially identical and arranged in a facing relationship to each other, as in <figref idref="f0003">Fig. 7</figref>, the breaking force required to break the frangible portion 16 will be substantially the same whether it is applied upwardly or downwardly, which makes the break hinge "D" "bi-directional." If there is only one notch, the break hinge will be "uni-directional" in that the breaking strength will be different depending on whether the breaking force is applied in the direction of the notch or in the opposite direction.

0038The notches 18 are areas of decreased breaking strength, so the breaking strength of the frangible portion 16 is less about a "bi-directional" or "uni-directional" break hinge "D" than about any other line in the plane of the notches. For example, it would require a much greater breaking force to break the frangible portion 16 about a vertical line in the plane of the notches 18 (by holding the distal portion 14 stationary and pressing the proximal portion 12 to the left or right) because the material between the notches 18 provides for increased breaking strength.

0039The magnitude of the breaking force required to break the frangible portion 16 about the break hinge "D" depends in part on the size of the notch 18. In general, the required breaking force will decrease with a larger notch and increase with a smaller notch. Thus, the minimum breaking strength of the frangible portion 16 may be controlled by controlling the width (i.e., the arcuate extent) and the length (i.e., the dimension amount in the direction of the longitudinal axis "A") of the notch 18. In one embodiment, the frangible portion 16 is adapted such that it will not break until a sufficient breaking force is applied. Such an embodiment functions as a safety mechanism, because the implantable medical device 34 cannot be released until a minimum breaking force is applied by the medical professional.

0040As described previously, the breaking force may be applied by holding the distal portion 14 stationary and pressing the proximal portion 12, but there are many other ways of applying a breaking force. For example, a breaking force may be applied by holding the proximal portion 12 stationary and pressing on the distal portion 14 or by moving the proximal portion 12 and distal portion 14 in opposite directions to create a shear force at the frangible portion 16. Hence, those of ordinary skill in the art will appreciate that there are a number of ways to apply a breaking force, and the present invention is not limited to a particular method of applying a breaking force.

0041When the frangible portion 16 has been broken, the proximal portion 12 of the carrier member 10 is moved away from the distal portion 14, as shown in <figref idref="f0004">Fig. 8</figref>. The proximal portion 12 may be moved along a path parallel to the longitudinal axis "A" of the carrier member 10, as shown in solid lines, or along a path at an angle to the longitudinal axis "A," as shown in broken lines. The locking member 20 is fixedly secured to the proximal portion 12, so this movement will retract the locking member 20. After sufficient retraction of the locking member 20, it will disengage the implantable medical device 34 and the detachment mechanism 28, which allows the kicker member 32 to return to a U-shaped condition, thereby deploying the implantable medical device 34 to the target location "B." Thereafter, the introducer 26 and the delivery system 24 are removed from the vasculature.

0042The foregoing description illustrates one method of using a delivery device according to the present invention, but other methods may also be used without departing from the scope of the present invention.

0043It will be seen from the preceding description that delivery systems according to the present invention eliminate numerous problems associated with known devices. In particular, delivery systems and associated methods of use according to the present invention ensure that the implantable device is completely separated from the engagement system and deployed to the target location. Further delivery systems according to the present invention may be manufactured in a simple, low-cost manner and do not require additional components, such as an attachable handle or re-zip sheath.