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1,032 catalysts · 1,000 device adverse event · 21 approval · 6 device 510k · 3 device pma · 2 grant
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1,032 catalysts · 1,000 device adverse event · 21 approval · 6 device 510k · 3 device pma · 2 grant
Patient Device Interaction Problem
Fracture
Degraded
Fracture
Degraded
Failure to Osseointegrate
Fracture
Adverse Event Without Identified Device or Use Problem
Device Stenosis
Therapeutic or Diagnostic Output Failure
Material Rupture
Inappropriate/Inadequate Shock/Stimulation
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Incorrect Interpretation of Signal
Patient Device Interaction Problem
Loosening of Implant Not Related to Bone-Ingrowth
Improper or Incorrect Procedure or Method
Loosening of Implant Not Related to Bone-Ingrowth
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Over-Sensing
Adverse Event Without Identified Device or Use Problem
Fluid/Blood Leak
Failure to Osseointegrate
Fluid/Blood Leak
Therapeutic or Diagnostic Output Failure
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Pumping Stopped
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Priming Problem
Adverse Event Without Identified Device or Use Problem
Patient Device Interaction Problem
Patient Device Interaction Problem
Failure to Osseointegrate
Osseointegration Problem
Fluid/Blood Leak
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Improper or Incorrect Procedure or Method
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate