Life Spine Receives US FDA’s 510(k) Clearance for ProLift Pivot Expandable Spacer System
Shots:
- The US FDA has granted 510(k) clearance to Prolift Pivot expandable spacer system, expanding Life Spine’s Micro Invasive tech portfolio
- The system provides full articulation for precise spinal fusion, while reducing tissue disruption & nerve retraction, allowing surgeons to restore patient alignment with superior control & efficiency. It also features OSSEO-LOC surface tech that promotes osseointegration & long-term implant stability
- Moreover, it offers the ability to collapse & expand (in-situ for ~5mm), full articulation for precise placement, a bulleted tip for easy insertion, reduced instrument passes, & in-situ graft delivery to ensure optimal alignment & reliability
Ref: Businesswire | Image: Life Spine
Related News:- Life Spine Reports the US FDA’s Approval of the ARx SAI Spinal Fixation System
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