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10,884 catalysts · 3,603 8k filing · 2,255 grant · 1,189 approval · 1,000 device adverse event · 890 device 510k · 641 device pma
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10,884 catalysts · 3,603 8k filing · 2,255 grant · 1,189 approval · 1,000 device adverse event · 890 device 510k · 641 device pma
Adverse Event Without Identified Device or Use Problem
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Infusion or Flow Problem; Material Twisted/Bent
Patient Device Interaction Problem
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Malposition of Device
Device Dislodged or Dislocated
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Material Separation
Adverse Event Without Identified Device or Use Problem
Use of Incorrect Control/Treatment Settings
Pumping Stopped
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Incorrect Interpretation of Signal
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Appropriate Term/Code Not Available
Insufficient Information
Material Fragmentation
Failure to Osseointegrate