Abstract: A plate assembly for attaching a bone flap to a skull is provided and may include a first plate member attached to the bone flap and a second plate member supported by the first plate member and movable between a retracted position and an extended position relative to the first plate member. The second plate member may be removed from a cut line between the bone flap and the skull in the retracted position and may extend over the cut line in the extended position.

Abstract: An implant assembly for a human sternum and ribs can include a sternal implant and a rib link. The sternal implant can be couplable to a sternum. The rib link can include a distal portion, a proximal portion, and a strut. The distal portion can be couplable to a rib. The proximal portion can be couplable to the sternal implant. The strut can connect the distal portion to the proximal portion. The strut can be configured to flex so that the distal portion can be aligned with the rib.

Abstract: A plate assembly for attaching a bone flap to a skull is provided and may include a first plate member attached to the bone flap and a second plate member supported by the first plate member and movable between a retracted position and an extended position relative to the first plate member. The second plate member may be removed from a cut line between the bone flap and the skull in the retracted position and may extend over the cut line in the extended position.

Abstract: A plate assembly for attaching a bone flap to a skull is provided and may include a first plate member attached to the bone flap and a second plate member supported by the first plate member and movable between a retracted position and an extended position relative to the first plate member. The second plate member may be removed from a cut line between the bone flap and the skull in the retracted position and may extend over the cut line in the extended position.

Abstract: An implant assembly for a human sternum and ribs can include a sternal implant and a rib link. The sternal implant can be couplable to a sternum. The rib link can include a distal portion, a proximal portion, and a strut. The distal portion can be couplable to a rib. The proximal portion can be couplable to the sternal implant. The strut can connect the distal portion to the proximal portion. The strut can be configured to flex so that the distal portion can be aligned with the rib.

Abstract: An implant assembly for a human sternum and ribs can include a sternal implant and a rib link. The sternal implant can be couplable to a sternum. The rib link can include a distal portion, a proximal portion, and a strut. The distal portion can be couplable to a rib. The proximal portion can be couplable to the sternal implant. The strut can connect the distal portion to the proximal portion. The strut can be configured to flex so that the distal portion can be aligned with the rib.

Abstract: A pressure port assembly and related components and methods are disclosed. In some instances, the pressure port assembly may comprise a pressure port body, including pressure port bodies composed of a continuous material. Pressure port bodies within the scope of this disclosure may be coupled to pressure sensing elements, including pressure transducers. Apertures or other flow paths may be provided across a pressure port body. Methods of integrally forming a pressure port body comprising a continuous material are also disclosed.

Abstract: An implant assembly for a human sternum and ribs can include a sternal implant and a rib link. The sternal implant can be couplable to a sternum. The rib link can include a distal portion, a proximal portion, and a strut. The distal portion can be couplable to a rib. The proximal portion can be couplable to the sternal implant. The strut can connect the distal portion to the proximal portion. The strut can be configured to flex so that the distal portion can be aligned with the rib.

Abstract: A closure system may secure a first bone portion to a second bone portion. The closure system may include a band, a locking terminal, and a tensioning device. The band may be adapted to be looped around the first and second bone portions. The locking terminal may fixedly engage a first portion of the band and selectively fixedly engage a second portion of the band. The tensioning device may include a body and a threaded rod. The threaded rod may be received in the body and may engage the band such that movement of the threaded rod relative to the body moves the second portion of the band relative to the first portion of the band.

Abstract: A closure system may secure a first bone portion to a second bone portion. The closure system may include a bracket, a band and a tensioning device. The bracket may include a first portion adapted to engage the first bone portion and a second portion adapted to engage the second bone portion. The band may engage the bracket and may be adapted to be looped around the first and second bone portions. The tensioning device may include a body and a threaded member. The threaded member may be received in the body and may engage the band such that rotation of the threaded member relative to the body moves a first end of the band relative to a second end of the band.

Abstract: A closure system may secure a first bone portion to a second bone portion. The closure system may include a bracket, a band and a tensioning device. The bracket may include a first portion adapted to engage the first bone portion and a second portion adapted to engage the second bone portion. The band may engage the bracket and may be adapted to be looped around the first and second bone portions. The tensioning device may include a body and a threaded member. The threaded member may be received in the body and may engage the band such that rotation of the threaded member relative to the body moves a first end of the band relative to a second end of the band.

Abstract: Sensor assemblies and related components and methods are disclosed. In some instances, the sensor assemblies include a sensor mounting body and a porous member. The porous member can be disposed within an aperture that extends through a sensor mounting body. The porous member may function as a dampening element or snubber that impedes the propagation of one or more pressure waves across the aperture. Some assemblies may include a metallized layer.

Abstract: A pressure port assembly and related components and methods are disclosed. In some instances, the pressure port assembly may comprise a pressure port body, including pressure port bodies composed of a continuous material. Pressure port bodies within the scope of this disclosure may be coupled to pressure sensing elements, including pressure transducers. Apertures or other flow paths may be provided across a pressure port body. Methods of integrally forming a pressure port body comprising a continuous material are also disclosed.

Abstract: A plate assembly for attaching a bone flap to a skull is provided and may include a first plate member attached to the bone flap and a second plate member supported by the first plate member and movable between a retracted position and an extended position relative to the first plate member. The second plate member may be removed from a cut line between the bone flap and the skull in the retracted position and may extend over the cut line in the extended position.

Abstract: A complex medical balloon (12) has at least two sections (14, 16), each of which has a different compliance curve. A compliance curve measures expansion size at various pressures. Accordingly, at a given pressure, one balloon section of a complex balloon will experience greater expansion than another section.

Abstract: The present invention consists of a main artery stent (the main stent) that is placed in the main artery and a second stent that is placed into the side branch (the side branch stent), the two stents constituting a complete treatment for a stenosed arterial bifurcation. Both stents are preferably drug eluting. The main stent would optimally be one that has a reasonably small area of each cell after the stent is deployed, but also has a large perimeter length for each cell. The stent delivery system for the side branch stent has an attached main guide wire tube that can be advanced over a main guide wire and a central lumen that is advanced over a guide wire placed into the side branch. The structure of the side branch stent delivery system allows the side branch stent to achieve the correct angular orientation and longitudinal position when it is advanced over the two guide wires.