| CPC A61F 2/4455 (2013.01) [A61B 17/1604 (2013.01); A61B 17/56 (2013.01); A61B 17/58 (2013.01); A61B 17/68 (2013.01); A61F 2/28 (2013.01); A61F 2/2803 (2013.01); A61F 2/2846 (2013.01); A61F 2/30767 (2013.01); A61F 2/30771 (2013.01); A61F 2/30907 (2013.01); A61F 2/32 (2013.01); A61F 2/38 (2013.01); A61F 2/40 (2013.01); A61F 2/4202 (2013.01); A61F 2/4225 (2013.01); A61F 2/447 (2013.01); A61F 2/4611 (2013.01); A61B 17/025 (2013.01); A61F 2002/2817 (2013.01); A61F 2002/2835 (2013.01); A61F 2002/30153 (2013.01); A61F 2002/30156 (2013.01); A61F 2002/30158 (2013.01); A61F 2002/30179 (2013.01); A61F 2002/30273 (2013.01); A61F 2002/30275 (2013.01); A61F 2002/3028 (2013.01); A61F 2002/30281 (2013.01); A61F 2002/30593 (2013.01); A61F 2002/30599 (2013.01); A61F 2002/30841 (2013.01); A61F 2002/30899 (2013.01); A61F 2002/30909 (2013.01); A61F 2002/30914 (2013.01); A61F 2002/3092 (2013.01); A61F 2/3094 (2013.01); A61F 2002/30943 (2013.01); A61F 2002/30952 (2013.01); A61F 2002/30953 (2013.01); A61F 2002/30957 (2013.01); A61F 2002/30962 (2013.01); A61F 2002/30968 (2013.01); A61F 2002/3097 (2013.01); A61F 2/36 (2013.01); A61F 2002/4628 (2013.01); A61F 2210/0076 (2013.01); A61F 2230/0063 (2013.01); A61F 2310/00011 (2013.01); A61F 2310/00017 (2013.01); A61F 2310/00023 (2013.01); A61F 2310/00029 (2013.01); A61F 2310/00047 (2013.01); A61F 2310/00179 (2013.01); A61F 2310/00598 (2013.01); A61F 2310/00796 (2013.01); A61F 2310/00958 (2013.01); A61F 2310/0097 (2013.01); A61F 2310/00976 (2013.01); B33Y 70/00 (2014.12); B33Y 80/00 (2014.12)] | 16 Claims |

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1. An implant for interfacing with a bone structure, comprising:
a web structure comprising a plurality of struts joined at nodes, wherein the web structure is configured to interface with human bone tissue;
a plurality of biocompatible fibers coated on one or more of the plurality of struts; and
a plurality of biodegradable particles contained within the biocompatible fibers, the biodegradable particles encapsulating one or more bone growth promoting agents, wherein the biodegradable particles dissolve in the presence of biological fluids in order to release the encapsulated bone growth promoting agents, and wherein the biodegradable particles include particles of varying sizes where different size particles release the encapsulated bone growth promoting at different times in the of the biological fluid.
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