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6,562 catalysts · 3,603 8k filing · 1,000 device adverse event · 775 grant · 578 earnings · 234 approval · 172 phase 2 completion
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6,562 catalysts · 3,603 8k filing · 1,000 device adverse event · 775 grant · 578 earnings · 234 approval · 172 phase 2 completion
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Premature Discharge of Battery
Loss of Osseointegration
Unable to Obtain Readings; Device Displays Incorrect Message
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Failure to Seal
Material Twisted/Bent
Material Twisted/Bent
Material Twisted/Bent
Material Twisted/Bent
Material Twisted/Bent
Adverse Event Without Identified Device or Use Problem
Obstruction of Flow; Infusion or Flow Problem
Appropriate Term/Code Not Available
Material Twisted/Bent
Adverse Event Without Identified Device or Use Problem
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Excess Flow or Over-Infusion
Patient-Device Incompatibility
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Failure to Osseointegrate
Obstruction of Flow
Low impedance
Migration
Impedance Problem
Unexpected Therapeutic Results
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Difficult to Advance; Patient Device Interaction Problem
Difficult to Remove
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem