A61F2002/30677

HIGH-PROFILE, ANATOMY-SPECIFIC CRANIOFACIAL IMPLANTS FOR COMBINED HARD AND SOFT TISSUE RECONSTRUCTION WITH EMBEDDED TECHNOLOGY FOR MEDICINE DELIVERY
20220047378 · 2022-02-17 · ·

An anatomy-specific implant for neuroplastic surgery. The implant includes a soft tissue implant component designed within and adapted to replace or restore missing soft tissue in a skull, joint or spine of the patient, wherein the soft tissue implant component is adapted to be coupled by an interdigitated connection to a rigid component. The rigid component can be a skull implant adapted to replace missing cranial or vertebral bone, or healthy cranial or vertebral bone, either of which can have downward extending catheters for medicinal brain or spinal cord infusion to help bypass the blood-brain barrier via multiphase flow. The soft tissue implant may include a functional component having neurotechnologies such as MRI-lucent pumps, Bluetooth connection systems, refillable diaphragms, remote imaging devices, wireless charging capabilities, and/or informative biosensors. The soft tissue implant component may be interchangeable with another soft tissue implant component in plug-and-play fashion.

System And Method For Treatment And Prevention Of Periprosthetic Joint Infections

Provided herein are rapid and effective local infection therapy methods, systems, and devices that significantly reduce the mortality, morbidity, and the cost of care in rare musculoskeletal infections. Continuous delivery of antibiotic therapy locally, at the infection site, reduces edema and provides antibiotic irrigation, significantly improving outcomes while reducing the need for systemic antibiotics.

Expandable support device and method of use

An expandable support device for tissue repair is disclosed. The device can be used to repair hard or soft tissue, such as bone or vertebral discs. The device can have multiple flat sides that remain flat during expansion. A method of repairing tissue is also disclosed. Devices and methods for adjusting (e.g., removing, repositioning, resizing) deployed orthopedic expandable support devices are also disclosed. The expandable support devices can be engaged by an engagement device. The engagement device can longitudinally expand the expandable support device. The expandable support device can be longitudinally expanded until the expandable support device is substantially in a pre-deployed configuration. The expandable support device can be then be physically translated and/or rotated.

Method for producing a spacer and hollow mold for producing a spacer
09770355 · 2017-09-26 · ·

A method for producing a spacer for insertion as a placeholder for an articular endoprosthesis, whereby a cement is filled into a compressed hollow space of a flexible compressed hollow mold, whereby the flexible hollow mold is expanded by the cement flowing into it, and the cement is filled into the hollow mold until the hollow space is expanded to a final state, whereby the hollow space in its final state determines the shape of the spacer to be produced, and the cement is then cured in said hollow space, and the spacer produced from the cement is removed from the hollow mold after curing. The invention also relates to the hollow mold, which comprises the compressible hollow space, whereby the hollow mold comprises at least one filling opening through which cement can be filled into the hollow space.

Silicone nucleus implants

A nucleus implant includes a core (10) arranged inside a nucleus pulposus space (Es) obtained after nucleotomy of the intervertebral disk (Di) and at least one extension (11) penetrating inside at least one channel (Co) formed in the vertebral body of the corresponding vertebra (Va, Vb) to strengthen and ensure a connection between the nucleus implant (1) and the bone body of the vertebra (Va) and/or (Vb) through the diffusion or migration of the viscoelastic material making up the nucleus implant in the cancellous bone of the vertebra.

Implant with deployable blades

An implant, comprising a body having a superior surface and an inferior surface, a superior-inferior axis, and a lateral axis. The implant further includes a first blade having a first retracted position in the body and a first extended position where the first blade extends outwardly from the body. In addition, the implant may include a blade actuating member that can translate through the body in directions parallel to the lateral axis. When the blade actuating member is moved in a first direction along the first axis, the first blade moves towards the first extended position. When the blade actuating member is moved in a second direction opposite the first direction, the first blade moves towards the first retracted position. Further, in the first extended position, the first blade extends from the superior surface at a first non-zero angle with respect to the superior-inferior axis.

EXPANDABLE SUPPORT DEVICE AND METHOD OF USE

An expandable support device for tissue repair is disclosed. The device can be used to repair hard or soft tissue, such as bone or vertebral discs. A method of repairing tissue is also disclosed. The device and method can be used to treat compression fractures. The compression fractures can be in the spine. The device can be deployed by compressing the device longitudinally resulting in radial expansion.

ABSORBING ELUTING SPACER DEVICE
20170319345 · 2017-11-09 ·

Disposable temporary spacer device for an articulation of the human body or for a bone cavity, wherein the spacer device includes at least one first component adapted to be constrained to a bone portion or end, wherein the spacer device is made from a biologically compatible material and comprises interconnected pores distributed in the entire volume occupied by the spacer device, in which the interconnected pores have a size and occupy a percentage of the volume of the spacer device such that it is able to absorb and consequently elute one or more pharmaceutical or medical substances in liquid or fluid form or in paste, cream, gel, wax, or viscous form.

Assembled implant

This invention is directed to an assembled implant comprising two or more portions of bone that are held together in appropriate juxtaposition with one or more biocompatible pins to form a graft unit. Preferably, the pins are cortical bone pins. Typically, the cortical pins are press-fitted into appropriately sized holes in the bone portions to achieve an interference fit. The bone portions are allograft or xenograft.

Methods and devices for utilizing bondable materials

The invention primarily relates to fastening and stabilizing tissues, implants, and/or bondable materials, such as the fastening of a tissue and/or implant to a bondable material, the fastening of an implant to tissue, and/or the fastening of an implant to another implant. This may involve using an energy source to bond and/or mechanically to stabilize a tissue, an implant, a bondable material, and/or other biocompatible material. The invention may also relate to the use of an energy source to remove and/or install an implant and/or bondable material or to facilitate solidification and/or polymerization of bondable material.