Inari Medical, Inc. has announced the FlowTriever System has received FDA 510(k) clearance for the treatment of pulmonary embolism (“PE”). This clearance makes the FlowTriever System the first and only thrombectomy device cleared by the FDA for the treatment of PE. The PE-specific clearance was based upon the strength of the recently released results from the FlowTriever Pulmonary Embolectomy (“FLARE”) Clinical Study.