A spinal interbody device (IBD) includes a solid wall that at least partially defines a boundary of the IBD and a porous body connected to the solid wall. The porous body includes a plurality of sections that form at least a portion of both a superior and inferior bone interface side of the IBD. Each section of the porous body has a different porosity than an adjacent section such that the porosities increase toward a center of the IBD.

A spinal interbody device (IBD) includes a solid wall that at least partially defines a boundary of the IBD and a porous body connected to the solid wall. The porous body includes a plurality of sections that form at least a portion of both a superior and inferior bone interface side of the IBD. Each section of the porous body has a different porosity than an adjacent section such that the porosities increase toward a center of the IBD.

A surface-reconfiguration implant, a method of using the surface-reconfiguration implant, and a method of implantation of the surface-reconfiguration implant that creates an articular surface between an upper portion of a humeral head and a greater tuberosity, and an undersurface of an acromion in shoulders with massive rotator cuff tears is provided. The surface-reconfiguration implant can include a body portion including at least an undersurface and an articular surface, where the undersurface is configured to interface with portions of a proximal humerus to facilitate attachment of the body portion thereto, and portions of the articular surface extend to and/and preferably beyond a normal anatomical shape of portions a humeral head and a greater tuberosity both superiorly and medially when the body portion is attached to the proximal humerus.

The device for maintaining an intervertebral space is capable of being accommodated inside the disc, in place of the core. Natural anchoring is ensured by promoting the regrowth of fibre around at least part of the device. The possibility of ejection of the residual core is limited in order to avoid a renewed hernia, and mobility of the vertebral column is ensured. To this end, a subject of the invention is a device having at least two non-expansible concentric rings which between them form a free space and which are connected to each other via two junction summits.

An implant includes a central wall extending from a first side of a peripheral frame portion to a second side of the peripheral frame portion, and a first helical bone contacting member attached at the central wall and disposed within the superior half of the implant. The implant further includes a first support member attached at the central wall at a junction coincident with the first helical bone contacting member and extending to a central region of the implant internal to the first helical bone contacting member. In addition, the implant includes a non-helical bone contacting member extending from a portion of the first support member that is disposed internal to the first helical bone contacting member.

A spinal interbody device (IBD) includes a solid wall that at least partially defines a boundary of the IBD and a porous body connected to the solid wall. The porous body includes a plurality of sections that form at least a portion of both a superior and inferior bone interface side of the IBD. Each section of the porous body has a different porosity than an adjacent section such that the porosities increase toward a center of the IBD.

A spinal interbody device (IBD) includes a solid wall that at least partially defines a boundary of the IBD and a porous body connected to the solid wall. The porous body includes a plurality of sections that form at least a portion of both a superior and inferior bone interface side of the IBD. Each section of the porous body has a different porosity than an adjacent section such that the porosities increase toward a center of the IBD.

An implant includes a central wall extending from a first side of a peripheral frame portion to a second side of the peripheral frame portion, and a first helical bone contacting member attached at the central wall and disposed within the superior half of the implant. The implant further includes a first support member attached at the central wall at a junction coincident with the first helical bone contacting member and extending to a central region of the implant internal to the first helical bone contacting member. In addition, the implant includes a non-helical bone contacting member extending from a portion of the first support member that is disposed internal to the first helical bone contacting member.

The device for maintaining an intervertebral space is capable of being accommodated inside the disc, in place of the core. Natural anchoring is ensured by promoting the regrowth of fibre around at least part of the device. The possibility of ejection of the residual core is limited in order to avoid a renewed hernia, and mobility of the vertebral column is ensured. To this end, a subject of the invention is a device having at least two non-expansible concentric rings which between them form a free space and which are connected to each other via two junction summits.

A surface-reconfiguration implant, a method of using the surface-reconfiguration implant, and a method of implantation of the surface-reconfiguration implant that creates an articular surface between an upper portion of a humeral head and a greater tuberosity, and an undersurface of an acromion in shoulders with massive rotator cuff tears is provided. The surface-reconfiguration implant can include a body portion including at least an undersurface and an articular surface, where the undersurface is configured to interface with portions of a proximal humerus to facilitate attachment of the body portion thereto, and portions of the articular surface extend to and/and preferably beyond a normal anatomical shape of portions a humeral head and a greater tuberosity both superiorly and medially when the body portion is attached to the proximal humerus.