Abstract: A medical device localization assembly includes an exterior frame, at least one lateral bar, a plurality of locating members and a targeting guide. The exterior frame includes a distal face configured to compress against tissue. The at least one lateral bar extends within the exterior frame and at least one open recess is formed between the lateral bar and the exterior frame. The plurality of locating members are positioned along an inner side of the exterior frame and the at least one lateral bar. The plurality of locating members extend into the at least one open recess and the at least one open recess is configured to removably receive the targeting guide at the proximal face. The plurality of locating members are sized and shaped to removably hold the guide cube such that the plurality of locating members are configured to correspond to the shape of the targeting guide.

Abstract: A biopsy device includes a body, a needle, a cutter, and a tissue sample holder. The needle extends distally from the body. The cutter is longitudinally translatable relative to the needle and defines a cutter lumen. The tissue sample holder includes a rotatable member, an individual sample tray, and one or more bulk sample trays. The rotatable member defines a single chamber partially divided by a plurality of tray protrusions extending radially inwardly from a cylindrical wall of the rotatable member. The individual sample tray includes a single sample chamber that is configured to receive a single tissue sample. The bulk sample tray is configured to receive a plurality of tissue samples.

Abstract: A marker delivery device includes a cannula with a first end, a second end, a marker exit near the second end, a handle into which the cannula extends or to which the cannula is attached, the cannula being capable of receiving a plunger and rod that are operable to deploy a marker from the marker exit, the marker delivery device further including a tapered adaptor portion attached to or surrounding the cannula and abutting the handle. The tapered adaptor portion is configured to engage a plurality of different sleeves for differing biopsy devices. Various aspects offer improved ease of removal from commercially available biopsy devices due to its “pinch release” feature. Various aspects of the device allow use with multiple commercially available biopsy devices so as to ensure proper positioning of the devices for marker deployment.

Abstract: A sterile cover assembly is for a biopsy device. The biopsy device includes a reusable holster including a housing and driving mechanism. The driving mechanism is for driving a cutter in a needle of a probe. The housing is adapted to releasably couple to the probe. The sterile cover assembly includes a sleeve and a flexible sterile cover. The sleeve is configured to receive at least a portion of the housing of the reusable holster. The sterile cover is coupled to the sleeve and is configured to cover the housing of the holster.

Abstract: A biopsy system with a grid plate used as either a lateral or medial compression plate of a localization fixture used with a breast coil includes a rotatable guide cube that may be inserted into a desired rectangular recess in the grid plate after rotating to position a selected guide hole in the desired spatial orientation. Versions of a guide cube include those rotatable in two axes to provide additional hole positions, angled holes, enlarged circular holes that function with a rotating guide to support a noncircular biopsy instrument cannula (e.g., trocar/sleeve combination, core biopsy probe of a biopsy device) for rotation. A rotating guide may have an unlocked state for easily sliding to a selected longitudinal position thereon. Thereafter, the rotating guide is locked to serve as a positive depth stop (e.g., quarter turn locking elastomeric rings, triangular and scissor clips, and shutter depth stops).

Abstract: A biopsy system, including a probe set, a holster, and a user interface. The probe set includes a plurality of probes. Each probe of the probe set includes a probe body, a needle, a cutter, and a tissue sample holder. The tissue sample holder is in communication with the cutter to receive one or more tissue samples. The holster is selectively securable to each probe of the probe set. The user interface is in communication with the holster. The user interface includes a display. The user interface is configured to identify which probe of the probe set is secured to the holster when a selected probe of the probe set is secured to the holster.

Abstract: An apparatus for individually storing multiple tissue samples separately from each other includes a base, a lid, a lock, and one or more vents. The base defines a plurality of reservoirs and a plurality of identification areas. A portion of the base defines an opening corresponding to each reservoir. The lid is configured to secure the multiple tissue samples within a corresponding reservoir by enclosing each corresponding opening in the closed configuration. The lock is configured to selectively lock the lid against the base in the closed configuration. The one or more vents are configured to enable entry of fluid into the reservoirs when the lid is in the closed configuration. The one or more vents are further configured to prevent exit of tissue samples from the reservoirs when the lid is in the closed configuration.

Abstract: A biopsy system comprises an introducer, a biopsy device having a needle, and a marker applier. The introducer may include a closed distal tip, a lateral aperture, a proximally facing interior wall, and a ramp that guides the closed distal end of a marker applier up and into abutment with the wall as the applier is fed into the introducer. The needle of the biopsy device includes a blunt distal end and features providing clearance for the ramp as the blunt distal end is brought into abutment with the wall when the needle is fed into the introducer. The introducer may alternatively include an open distal end having resiliently biased leaves that bear against an inserted biopsy device needle. In some other versions, a fin projects laterally from the closed distal end of a marker applier, spacing the distal end away from a sidewall region of the introducer cannula.

Abstract: A biopsy device comprises a body, a needle, a cutter, and a valve assembly. The needle extends distally relative to the body. The needle defines a first lumen and a second lumen. The first and second lumens extend along a first and second longitudinal axis, respectively. The needle includes an opening fluidly coupling the first and second lumens. The cutter is translatable relative to the needle. The valve assembly comprises a vent opening and a spool body. The spool body is movable relative to the vent opening between a first and second position. The second lumen is coupled to the vent opening when the spool body is in the first position. The second lumen is sealed relative to the vent opening when the spool body is in the second position. The spool body is configured to transition between the first and second position by translation of the cutter.

Abstract: A biopsy system, including a biopsy device, a localization assembly, and a control module. The localization assembly is configured to orient the biopsy device relative to a patient. The control module is communication with the biopsy device. The control module is configured to operate a plurality of functional features of the biopsy device. The control module includes a cable and a cable management assembly. The cable management assembly includes a pair of cable management plates, and a weight. Each of the pair cable management plates are disposed substantially parallel to each other and define a space therebetween. The weight is configured to move within the space defined by the pair of cable management plates. The weight is attachable to the cable of the control module and is further configured to slide axially along the cable.

Abstract: A handheld biopsy device comprises a handpiece, a fluid collection system, and a power transmission source. The handpiece is configured for grasping by a single hand and is independently manipulatable by hand for movement of the instrument toward and away from the patient. An elongated piercer extends from the distal end of the handpiece. The piercer has a sharpened distal end and a port located proximal to the distal end for receiving a portion of tissue mass. An elongated cutter is disposed coaxially relative to a piercer lumen of the piercer. A distal blade of the cutter slides distally past the port of the piercer to severe the tissue portion drawn into the port by vacuum. The handpiece further comprises a holster for detachably connecting a cutter rotation transmission and a cutter axial transmission to the power transmission source.

Abstract: A tool for inserting a marker into tissue at a biopsy site includes an elongate plunger having a blind bore. A plunger rod has a proximal end received within and secured to the blind bore so that the plunger rod moves conjointly with the plunger and a spring is secured to the distal end of the plunger rod. A cannula has a lumen that receives a distal end of the plunger rod and a crimp is formed in the cannula near its distal end. The cannula has a side exit port where a marker is ejected from the lumen. A ramp is formed in communication with the side exit port and the ramp has a preselected slope that controls the angle at which the marker is ejected. The marker is ejected from the side exit port into tissue when the spring unloads abruptly as the marker clears the crimp.

Abstract: A needle for use with a biopsy device is described and claimed. The needle is manufactured using a metal injection molding or “MIM” process. The needle includes a piercing tip, wherein the piercing tip includes a base portion, a first cutting portion and a second cutting portion, wherein the first cutting portion and the second cutting portion extend distally from the base portion, wherein the base portion defines a first diameter, wherein the first diameter of the base portion corresponds to the first diameter of the cannula, wherein the first cutting portion defines a first cutting edge and a second cutting edge, wherein at least a portion the first cutting edge and at least a portion of the second cutting edge extends outwardly beyond the first diameter of the base portion.

Abstract: A biopsy system with a grid plate used as either a lateral or medial compression plate of a localization fixture used with a breast coil includes a rotatable guide cube that may be inserted into a desired rectangular recess in the grid plate after rotating to position a selected guide hole in the desired spatial orientation. Versions of a guide cube include those rotatable in two axes to provide additional hole positions, angled holes, enlarged circular holes that function with a rotating guide to support a noncircular biopsy instrument cannula (e.g., trocar/sleeve combination, core biopsy probe of a biopsy device) for rotation. A rotating guide may have an unlocked state for easily sliding to a selected longitudinal position thereon. Thereafter, the rotating guide is locked to serve as a positive depth stop (e.g., quarter turn locking elastomeric rings, triangular and scissor clips, and shutter depth stops).

Abstract: A biopsy device comprises a probe body, a needle portion, a hollow cutter, and a tissue sample holder. The needle portion extends distally from the probe body and comprises a transverse tissue receiving aperture. The hollow cutter is translatable relative to the needle portion to sever a tissue sample from tissue protruding though the aperture. The hollow cutter defines a cutter lumen. The tissue sample holder comprises a body and a tissue sample tray. The tissue sample tray is removably engaged with the body and comprises a downwardly extending lumen. The downwardly extending lumen includes a pair of lower openings which are in communication with a chamber defined by the tissue sample tray.

Abstract: A biopsy system includes a biopsy device, a control module, a control module interface, at least one wireless data communication link, and an encoder. The biopsy device is operable to capture a tissue sample and includes a reusable portion and a disposable portion. The reusable portion includes an MR compatible motor. The disposable portion is adapted to be releasably joined with the reusable portion. The control module interface is configured to provide an interface between the control module and the reusable portion of the biopsy device. The at least one wireless data communication link includes a first data link configured to permit communication of data between the reusable portion of the biopsy device and the control module interface. The encoder is operationally coupled with the MR compatible motor.

Abstract: A biopsy device includes a probe, a holster, and a tissue sample holder for collecting tissue samples. The probe includes a needle and a hollow cutter. The tissue sample holder includes a housing having one or more chambers that are configured to receive a removable tray including one or more prongs and a bulk chamber of a different volume than the one or more chambers. The housing is releasably engageable with the probe. Each tray prong is configured to receive a tissue sample communicated through the cutter lumen. The tray is removable from the housing, such as along an axial direction. The tissue sample holder is rotatable to successively index each chamber to the cutter lumen. The trays may be flexible, resilient, or rigid.

Abstract: Methods for localizing a biopsy site are disclosed. The method includes taking a tissue sample from a biopsy site and positioning a detectable, bioabsorbable element at the biopsy site at the time that the tissue sample was taken. The tissue sample is then tested. The biopsy site is then relocated by finding the bioabsorbable element. The bioabsorbable element may be made of collagen, gelatin, cellulose, polylactic acid, and/or polyglycolic acid. The detectable bioabsorbable element may be relocated using ultrasound or mammography. The bioabsorbable element may also swell upon contact with body fluid.

Abstract: A biopsy device includes a body, a needle, and a cutter. A motor is operable to both move the cutter relative to the needle and actuate a needle firing assembly to retract and fire the needle relative to the body. The biopsy device also includes a needle rotation assembly that is configured to substantially prevent rotation of the needle about the longitudinal axis when the needle is in a proximal position yet permit rotation of the needle about the longitudinal axis when the needle is in a distal position. A valve assembly of the biopsy device includes a slider that selectively couples a secondary lumen in the needle with either atmospheric air or saline based on the longitudinal position of the slider. The cutter passes through the slider.