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20,074 catalysts · 4,728 grant · 3,700 8k filing · 2,716 approval · 2,690 device 510k · 2,000 device recall · 1,894 device pma
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20,074 catalysts · 4,728 grant · 3,700 8k filing · 2,716 approval · 2,690 device 510k · 2,000 device recall · 1,894 device pma
Loss of Osseointegration
Fluid/Blood Leak; Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Malposition of Device
Pumping Stopped
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Use of Device Problem
Adverse Event Without Identified Device or Use Problem
Device Dislodged or Dislocated
High impedance; Capturing Problem
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Premature Discharge of Battery
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Degraded
Capturing Problem
Over-Sensing
No Audible Prompt/Feedback
Over-Sensing
Detachment of Device or Device Component; Material Split, Cut or Torn
Insufficient Information
Loss of Osseointegration
Insufficient Information
Unable to Obtain Readings; Device Displays Incorrect Message
Fracture
Fracture
Energy Output Problem
Patient Device Interaction Problem
Patient-Device Incompatibility
Loss of Osseointegration
High Readings
Material Deformation; Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Failure to Deflate
Pumping Stopped
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Patient Device Interaction Problem
Fracture
Degraded
Fracture
Degraded