A separator element (300) is designed to prevent the passage of granulate along an axial direction (L) but to allow the passage of liquid along the axial direction (L). The separator element (300) has an internal thread (310) open towards its proximal end, and an external thread (320) open towards the distal end. At its proximal end, the separator element additionally has at least one resilient locking arm (330) which is arranged on the outer circumference and winch extends with its free end in the proximal direction. In this way, the separator element can be mounted on the discharge opening of a container (100) and, by means of a closure piece (400), can be fixed on the container in such a way that the separator element remains on the container when the closure piece is removed.

A adaptor is used with a driver, a drill, and a cannula to facilitate removal of material from bone and placement of the cannula in the bone. The adaptor includes an end portion provided at a proximal first end that is configured to engage a portion of the drill; a body portion attached to the end portion and extending from the end portion toward a distal second end; a head portion provided at the distal second end and attached to the body portion; and a passageway for receiving the drill that extends through the adaptor. Furthermore, the head portion includes a distal surface and at least one coupler provided on or adjacent the distal surface for releasably engaging, the cannula.

An apparatus for fixating bone includes an orthopedic implant. The orthopedic implant may be manufactured from a shape memory material such that the orthopedic implant is moveable between a natural shape and an insertion shape. The orthopedic implant defines at least a first cannulation therethrough adapted to deliver a bone augmentation material to the bone. The orthopedic implant implants into the bone in its insertion shape. After implantation of the orthopedic implant, the first cannulation facilitates delivery into the bone of a bone augmentation material that augments the bone. The orthopedic implant once implanted attempts to transition from its insertion shape to its natural shape such that the orthopedic implant fixates the bone.

A handle device is provided comprising a first wing and a second wing. The first wing and the second wing are configured to pivot about a common axis to one another. The first wing has one or more first ridge, and a first one or more clearance spaces. The second wing has one or more second ridges and a second one or more clearance spaces. The one or more first ridges is configured to be received within the second one or more clearance spaces and the one or more second ridges is configured to be received within the first one or more clearance spaces when the first wing is pivoted about the common axis to the second wing in a folded configuration.

A medical balloon device includes an outer member extending along an axis. An inflatable member has a proximal end extending from a first end of the outer member and a distal end. An inner member is positioned within the outer member and the inflatable member such that a first end of the inner member is coupled to the distal end of the inflatable member. A support member is movably disposed within the inner member and includes a first end configured to removably engage the first end of the inner member. Translation of the support member along the axis causes the inflatable member to move between a first position in which the inflatable member has a first length and a first profile and a second position in which the inflatable member has a second reduced length and a second reduced profile. Methods of use are disclosed.

The bioinjection device has a housing including a pistol grip and an elongated barrel. A trigger is pivotally mounted to the housing. An inner shaft having a distal end is slidable between a first position in which the distal end of the inner shaft is disposed in the barrel and a second position in which the distal end of the inner shaft extends past an opening in the end of the barrel. A tip containing a medicament is disposed about the opening of the elongated barrel. The tip includes at least one aperture for dispensing the medicament. One can inject the medicament from the tip into a bone fracture or degenerative bone tissue during surgery by actuating the trigger of the bioinjection device. A configurable tip may be employed to control the amount and direction of dispersion of such medicament.

A surgical method includes accessing a depressed bone fragment of a depression fracture with a surgical assembly. The surgical assembly includes a cannula and an obturator receivable through the cannula. The method further includes positioning the depressed bone fragment toward its original anatomical position using a blunt tip of the obturator. The method also includes injecting a liquid repair material through the cannula to the depression fracture to repair the depression fracture.

A bone fastener includes a shaft. The shaft includes a wall that defines a longitudinal cavity and a plurality of openings in communication therewith. The openings are disposed in axial alignment along the shaft and the wall is closed exclusive of the openings. In some embodiments, systems, spinal constructs, surgical instruments and methods are disclosed.

A kyphoplasty system includes various instruments which can be selectively used in a surgical theater (e.g., during a surgical operation on a patient) or a surgical training environment. The kyphoplasty system can include one or more of a kyphoplasty apparatus, a prone table mat, a connector system, a bone introducer needle, and a biopsy device. The kyphoplasty system may also include a training system for use in the training environment.

Systems and methods for stabilizing a bone structure of a patient. A stylet and a delivery tube is directed through an access cannula to form a curved path to a target site. The stylet is withdrawn with a distal portion of the flexible delivery tube maintaining a curved configuration along the curved path. The curable material including a plurality of elements disposed in a fluent material is directed through the flexible delivery tube with a distal portion of the flexible delivery tube maintaining the curved configuration against forces from the elements and the fluent material. A delivery cannula may be directed through the flexible delivery tube. An expandable member may deployed at the target site to create a cavity. A steerable assembly may be selectively activate to form the curved path. The plurality of elements may substantially follow a curved path created within the bone structure.