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21,617 catalysts · 4,728 grant · 3,706 8k filing · 3,653 device 510k · 2,971 approval · 2,000 device pma · 2,000 device recall
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21,617 catalysts · 4,728 grant · 3,706 8k filing · 3,653 device 510k · 2,971 approval · 2,000 device pma · 2,000 device recall
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
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