Jupiter Endovascular wins 510(k) FDA clearance for Vertex catheter

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Jupiter Endovascular’s Vertex™ Catheter just received 510(k) clearance for the insertion of endovascular devices.

This technology adopts Transforming Fixation (TFX) — able to shift from flexible to firm on demand, giving physicians true stability and control.

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K252027

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