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21,314 catalysts · 4,728 grant · 3,704 8k filing · 3,460 device 510k · 2,894 approval · 2,000 device pma · 2,000 device recall
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21,314 catalysts · 4,728 grant · 3,704 8k filing · 3,460 device 510k · 2,894 approval · 2,000 device pma · 2,000 device recall
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
Failure to Osseointegrate
Wireless Communication Problem
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Therapeutic or Diagnostic Output Failure
Adverse Event Without Identified Device or Use Problem
Therapeutic or Diagnostic Output Failure
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Unable to Obtain Readings; Device Displays Incorrect Message
Inappropriate/Inadequate Shock/Stimulation; Device Sensing Problem
Adverse Event Without Identified Device or Use Problem
Crack; Fluid/Blood Leak
Infusion or Flow Problem
Adverse Event Without Identified Device or Use Problem
Material Split, Cut or Torn
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate