US2016000489A1PendingUtilityA1

Composite Metal and Bone Orthopedic Fixation Devices

Assignee: STC UNMPriority: Jun 15, 2012Filed: Sep 15, 2015Published: Jan 7, 2016
Est. expiryJun 15, 2032(~5.9 yrs left)· nominal 20-yr term from priority
A61B 17/864A61B 17/866A61B 17/7035A61B 17/8625A61B 17/8615A61B 17/8685A61B 17/7002A61F 2310/00958A61F 2310/00359A61B 17/8841A61F 2002/30601A61B 17/8605A61F 2310/00023A61F 2002/2835A61B 17/702A61B 17/7098A61F 2002/3055A61B 17/68A61F 2310/0097A61B 17/7037A61B 2017/00933A61B 17/80A61F 2002/30784A61F 2002/30405A61B 2017/00964A61F 2/44A61F 2002/30787
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Claims

Abstract

Composite orthopedic devices that facilitate spine stabilization, such as: bone screws, rods, plates, interbodies, and corpectomy cages are disclosed. They are designed to provide both strength and load carrying capabilities, while increasing bio-integration of the devices with the surrounding bone tissue. They are constructed of composite layers of allograft and/or autograft bone and a structural material, such as titanium alloy or carbon/graphite fiber composite. Cannulations within the device are loaded with a mixture of stem cells, particles of allograft and/or autograft bone, and bone growth factors, such as BMP-2. The cannulations are connected to the surface of the device via multiple fenestrations that provide pathways to supply the bone/stem cell mixture to the surface, allowing living bone tissue to grow and insure bio-integration. The devices can also have radiofrequency (RF) stimulation implantation within the structure of the implanted device, capable of responding to external RF stimulation of enhanced bone growth.

Claims

exact text as granted — not AI-modified
1 - 11 . (canceled) 
     
     
         12 . A composite orthopedic rod for use in a surgical procedure comprising a shaft having a first end and a second end wherein the shaft defines a cannulation extending along at least a portion of the length of the shaft;
 wherein the cannulated portion of the shaft contains at least one fenestration,   wherein the rod is constructed of a material comprising allograft and/or autograft bone and a metal or metal alloy.   
     
     
         13 . The rod according to  claim 15 , wherein the rod is constructed of a material comprising a core and two layers; wherein the core is allograft and/or autograft bone, the middle layer is a metal or metal alloy, and the outermost layer is allograft and/or autograft bone. 
     
     
         14 . The rod according to  claim 15 , wherein the rod is constructed of a material comprising about 50% allograft and/or autograft bone and about 50% metal or metal alloy. 
     
     
         15 . The rod according to  claim 15 , wherein the metal or metal alloy is selected from the group consisting of titanium, cobalt-chromium, niobium alloy, and tantalum alloy. 
     
     
         16 . The rod according to  claim 15 , wherein the rod is coated with an antibiotic solution. 
     
     
         17 . The rod according to  claim 15 , wherein the cannulated portion of the shaft is filled with stem cells and allograft and/or autograft bone. 
     
     
         18 . The rod according to  claim 15 , wherein the titanium or metal products is replaced with carbon fiber product in exact ratio as described above with the titanium embodiment. 
     
     
         19 . The rod according to  claim 15 , further comprising radiofrequency stimulation implantation within the structure of the rod, capable of responding to external stimulation. 
     
     
         20 . A composite orthopedic rod for use in a surgical procedure comprising a shaft having a first end and a second end wherein the shaft defines a cannulation extending along at least a portion of the length of the shaft;
 wherein the cannulated portion of the shaft contains at least one fenestration; and   wherein the rod is constructed entirely of a carbon or graphite fiber reinforced composite material that essentially contains no metal or metal alloy.

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