Xtant Medical gained FDA 510(k) clearance for its InTiceâ„¢-C Porous Titanium Cervical Interbody System. InTice-C uses OsteoSync Ti, a highly porous titanium scaffold material that more closely resembles the bioscaffold of cancellous bone.
InTice-C is also cleared for use with Xtant’s proprietary allograft lines, including OsteoSponge®, 3Demin® Cortical Fibers, and OsteoViveâ„¢ viable cell allograft.
This is Xtant’s first spinal implant to use porous titanium.
Xtant Medical gained FDA 510(k) clearance for its InTiceâ„¢-C Porous Titanium Cervical Interbody System. InTice-C uses OsteoSync Ti, a highly porous titanium scaffold material that more closely resembles the bioscaffold of cancellous bone.
InTice-C is also cleared for use with Xtant's proprietary allograft lines, including OsteoSponge®, 3Demin®...
Xtant Medical gained FDA 510(k) clearance for its InTiceâ„¢-C Porous Titanium Cervical Interbody System. InTice-C uses OsteoSync Ti, a highly porous titanium scaffold material that more closely resembles the bioscaffold of cancellous bone.
InTice-C is also cleared for use with Xtant’s proprietary allograft lines, including OsteoSponge®, 3Demin® Cortical Fibers, and OsteoViveâ„¢ viable cell allograft.
This is Xtant’s first spinal implant to use porous titanium.
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