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18,593 catalysts · 4,728 grant · 3,686 8k filing · 2,620 approval · 2,122 device 510k · 1,717 device recall · 1,469 device pma
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18,593 catalysts · 4,728 grant · 3,686 8k filing · 2,620 approval · 2,122 device 510k · 1,717 device recall · 1,469 device pma
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Gradient Increase
Adverse Event Without Identified Device or Use Problem
High Capture Threshold
Device Appears to Trigger Rejection
Unexpected Therapeutic Results; Therapeutic or Diagnostic Output Failure
Unexpected Therapeutic Results; Therapeutic or Diagnostic Output Failure
Loss of Osseointegration
Intermittent Capture; High impedance
Loss of Osseointegration
Insufficient Information
Loss of Osseointegration
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
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Device Appears to Trigger Rejection
Intermittent Capture; High Capture Threshold
Patient Device Interaction Problem
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Failure to Interrogate; Communication or Transmission Problem
Detachment of Device or Device Component
Expulsion
Expulsion
Obstruction of Flow
Patient-Device Incompatibility
Patient-Device Incompatibility
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Signal Artifact/Noise; Electromagnetic Interference
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
Signal Artifact/Noise; Fracture
Patient Device Interaction Problem
Patient Device Interaction Problem
Material Rupture
Difficult to Remove
Insufficient Flow or Under Infusion