Providence Medical Technology's 3D-printed posterior cervical stabilization system, CORUS PCSS 3D-T, has completed its first commercial surgeries (at Adventist Health White Memorial in Los Angeles and Bon Secours in Virginia), less than a month after receiving FDA 510(k) clearance on October 13. The implant's core is a proprietary porous titanium lattice (mimicking cancellous bone), with 1.5 times more surface area and 8 times higher surface roughness than the original machined version, and is indicated for multi-level posterior fusion at C3-C7. Medical-grade titanium alloy powder (Ti-6Al-4V) is moving from 'approval' to 'actual clinical volume ramp-up' in the high-value spinal fusion consumables segment; as installation volume increases, batch consistency and traceability requirements for the powder will tighten accordingly. (First surgeries on 10/29, reported in November; Ada candidate inclusion)