Mould and method for realizing a temporary prosthesis of hip or shoulder, which comprises a shaft and a head. The mould comprises: a first mould portion (1) comprising a first half-shell (2); a second mould portion (3) comprising a second half-shell (4); the first mould portion (1) and the second mould portion (3) being able to be coupled with respect to each other so that the first and second half-shell (2, 4) are counter-faced and define a chamber (5) which conforms a shaft portion (5a), a head portion (5b) and an opening (5c) for injection of a fluid (preferably viscous) material; fixing means (6) for fixing the first and the second portion (1, 3); a first insert (7) comprising a cap portion (8) which is realized as a unique body, is dimensioned to be inserted in the head portion (5b) and is conformed to give shape to the head of the prosthesis. The first mould portion (1), the second mould portion (3) and the first insert (7) are mutually conformed to obtain a temporary prosthesis, when the first mould portion (1) and the second mould portion (3) are coupled together, the first insert (7) is inserted in the head portion (5b) and the fluid (preferably viscous) material is injected in the opening (5c).

The invention relates to a device for producing a spacer having a casting mold lower part (1) with a cavity (2), a casting mold wall (3) which extends peripherally away from an edge of the cavity (2) and which is open on the opposite side, a casting mold upper part (5) with a shaping surface (6), wherein the casting mold upper part (5) can be inserted into an interior (4) of the casting mold lower part (1) and is displaceable in the direction of the cavity (2), such that a hollow space is formed which is delimited by the cavity (2), the shaping surface (6) and the casting mold wall (3) and in which the spacer is moldable, at least one container (7) for receiving excess bone cement paste, and at least one opening (8) in the shaping surface (6) and/or in the cavity (2), which opens into the at least one container (7) for receiving excess bone cement paste.

The invention also relates to a method for producing spacers using such a device.

A mold for forming a joint spacer device or a part thereof includes a rigid container body having a first perimeter profile delimiting a first molding surface configured to shape a first portion of the joint spacer or part thereof; and a rigid cover provided with a second perimeter profile delimiting a second molding surface configured to shape a second portion of the joint spacer or part thereof. The rigid container body and the rigid cover are removably engageable to each other, at the first and the second perimeter profile, so as to delimit a cavity corresponding to the external configuration of the joint spacer or part thereof. The mold includes a weakening system on the rigid container body and on the rigid cover, making them separable into parts to enable the extraction of the spacer device or part thereof, molded therebetween.

Disclosed are interosseous cages interposed between two bones. The cage includes at least one body with two bearing faces each bearing face being configured so as to come into contact with the two bones, the body being produced from a first material having a given strength, a through cavity produced in the body opening onto the two faces and an insert defined between two end faces and having a cross section which is at most equal to the cross section of the through cavity, in a manner such that the insert is slid into the cavity, this insert furthermore being configured in a manner such that its end faces are respectively a continuation of the two faces when the insert is in the cavity, the insert being produced from a second material which is stronger than the first material. Application primarily to the production of intervertebral cages.

An implant for at least partially filling a bore hole in a bone includes a biocompatible plate and a support structure. The support structure has a ring-shaped inner support frame having an outer surface defining the outer diameter of the inner support frame and an inner surface, and an outer support frame having a plurality of fastening points adapted for attaching the implant to bone surrounding a bore hole in which the plate is inserted. The outer support frame is connected to and extends away from the outer surface of the inner support frame. A method of forming the implant is also provided.

A modular spacer device for a knee joint includes a tibial element adapted to be constrained to an end of the tibial bone and a femoral element adapted to be constrained to an end of the femoral bone and to be articulated on the tibial element. The tibial element has first and second surfaces opposite to each other, and the femoral element has first surface and second surfaces opposite to each other. The first surface of the femoral element is convex and laterally has a curved, ammonite-shaped contour with a curvature radius that increases starting from a rear section with a curvature radius R1, a first central section having a curvature radius R2, a second central section having a curvature radius R3, and a front section having a curvature radius R4, with R1≤R2≤R3≤R4.

A cranial implant for access to a cerebral cortex includes a window member shaped and dimensioned for positioning within a dural defect to provide access through the dura such that access to the cerebral cortex is provided in a location under study. An implant body is provided having a geometry that substantially conforms to a resected portion of a patient's anatomy to which the implant body is to be secured.

Additive-manufacturing systems for forming non-woven fibrous implants are disclosed. Additive-manufacturing systems may include a robotic subsystem having scanning and imaging equipment configured to scan a patient's anatomy, and an armature including at least one dispensing nozzle configured to selectively dispense at least one material. The system may further include a controller apparatus configured to send a control signal to control the scanning and imaging equipment to determine a target alignment of a patient's spine, and develop an additive-manufactured printing plan including an additive-manufactured material selection plan based on the target alignment of the patient's spine. The controller may execute the additive-manufactured printing plan to: dispense the at least one material to form a non-woven fibrous component. The non-woven fibrous component may define a plurality of randomly oriented fibers further defining a plurality of open pore spaces between adjacent fibers configured to facilitate boney ingrowth between adjacent fibers.

A cranial implant for access to a cerebral cortex includes a window member shaped and dimensioned for positioning within a dural defect to provide access through the dura such that access to the cerebral cortex is provided in a location under study. An implant body is provided having a geometry that substantially conforms to a resected portion of a patient's anatomy to which the implant body is to be secured.

An acetabular spacer device, of a type that is temporary and disposable, adapted to be implanted in use in a bone cavity placed at a joint of the human body, such as a hip or shoulder joint, has a cup-like shape, substantially hemispherical, and includes a first convex surface, adapted to be positioned at the bone cavity, a second concave surface, which defines a cavity, further includes at least one pharmaceutical or medical substance, such as at least one antibiotic, adapted to treat during use an ongoing infection in the bone cavity.