Provided herein are magnetic resonance imaging (MRI) compatible, convection-enhanced delivery (CED) cranial implant devices and related methods for performing a wide array of therapeutic and/or monitoring applications. In one aspect, the cranial implant device includes a cranial implant housing configured for intercranial implantation in a cranial opening of a subject. The cranial implant housing comprises a substantially anatomically-compatible shape, at least first and second surfaces, and at least one fluidic circuit comprising at least one cavity and at least one port that fluidly communicates with the cavity through at least the second surface, in which the cavity comprises, or is capable of comprising, at least one fluidic therapeutic agent. The device also includes at least one CED pump operably connected to the fluidic circuit, which CED pump is configured to convey the fluidic therapeutic agent from the cavity through at least one fluid conduit when the fluid conduit is operably connected to the port to maintain at least one positive pressure gradient of the fluidic therapeutic agent at least proximal to an outlet of the fluid conduit. In addition, the device also includes at least one power source operably connected at least to the CED pump. The cranial implant housing, the CED pump, and the power source are typically fabricated from one or more MRI compatible materials. Other aspects relate to various methods of treating a neurologically-related disease using the cranial implant devices, methods of monitoring therapeutic agent administration in a plurality of subjects, and methods of fabricating a cranial implant device as well as surgical methods.

A system and method is provided for imaging and monitoring a tissue, such as a cerebral cortex, of a subject. Access to imaging a tissue, such as cerebral cortex, may be provided by removing a portion of a bone, such as a portion of a skull of the subject. A prosthesis, such as an optically transparent prosthesis, may be used to replace the portion of the skull removed and may be conformed to the same 3D contour of the bone that was removed. A data acquisition system, such as an imaging system, may then be affixed to the skull prosthesis and may be used to acquire image data of the tissue of the subject at high spatial and temporal resolution and without interference from intervening bone material.

The present invention relates to a safety element, an implant comprising such a safety element and an implant system comprising an implant with the safety element. The safety element for an implant is arranged between an outer and inner part of an implant, wherein the safety element engages into the gearing of an expansion ring, wherein a releasing space between outer part and inner part of the implant is provided into that the safety element is to be radially moved for enabling rotation of the expansion ring.

A method for single-stage cranioplasty reconstruction includes prefabricating a clear craniofacial implant, creating a cranial, craniofacial, and/or facial defect, positioning the clear craniofacial implant over the cranial, craniofacial, and/or facial defect, tracing cut lines on the clear craniofacial implant as it lies over the cranial, craniofacial, and/or facial defect, cutting the prefabricated clear custom craniofacial implant along the hand-marked lines for optimal fit of the clear implant within the cranial, craniofacial, and/or facial defect, and attaching the final clear craniofacial implant to the cranial, craniofacial, and/or facial defect with standard fixation methods of today.

The present invention relates to a partial joint replacement (1000), encompassing a shell-like segment (100) with a concave inner contour (3) for the arrangement on at the bone structure of a patient, wherein the segment (100) comprises a lateral section (5) and a medial section (7) along a longitudinal direction (x), and wherein the outer contour (1) of the segment (100) comprise in longitudinal direction (x) at least one inflection point (9).

There is provided herein a surgical procedure for cancerous mandibular reconstruction and a temporary mandibular spacer therefor. The spacer is a structural load-bearing and rigid/stiff interim space maintenance device that can be used by surgeons to temporarily bridge the gap across a resected part of the mandible. The device may be made of a rigid and biocompatible polymer material which is anatomically shaped like a natural mandible. During surgery, the mandibular spacer may be quickly cut with a surgical saw into the desired lengths by the surgeon which may more precisely match the resected segment of native mandible. The length and the shapes of the terminal ends of the spacer may be configured to more precisely maintain the position of the remaining mandibular segments in their original locations and thus preserve the occlusion and surrounding soft tissues in their correct anatomical positions, reducing or eliminating scarring and/or malocclusion.

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.

A medical grade thermoplastic or polymer implant with an osteoconductive coating is provided, specifically for corrections of the distal and proximal interphalangeal toe joints of the foot. The implant can be either straight or angled, and can be either solid or cannulated for insertion. The implant is sized and shaped depending on the specific anatomy and desired correction. End portions of the implant may be coated with an osteoconductive coating that promotes bone growth, but may reduce radiolucency. Thus, a central portion of the implant may remain uncoated to increase radiolucency of the implant at the region where two bones come together.

The present invention relates to an assembly for imaging and/or treating brain tissue, having at least one acoustic window (10) which comprises a plate (1) that is transparent to ultrasonic waves, and at least one positioning marker (2) which facilitates positioning of a probe for generating ultrasonic waves so as to be aligned with said acoustic window (10).

The present invention relates to a partial joint replacement (1000), encompassing a shell-like segment (100) with a concave inner contour (3) for the arrangement on at the bone structure of a patient, wherein the segment (100) comprises a lateral section (5) and a medial section (7) along a longitudinal direction (x), and wherein the outer contour (1) of the segment (100) comprise in longitudinal direction (x) at least one inflection point (9).