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10,884 catalysts · 3,603 8k filing · 2,255 grant · 1,189 approval · 1,000 device adverse event · 890 device 510k · 641 device pma
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10,884 catalysts · 3,603 8k filing · 2,255 grant · 1,189 approval · 1,000 device adverse event · 890 device 510k · 641 device pma
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Fracture
Fluid/Blood Leak
Fluid/Blood Leak
Insufficient Information
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Signal Artifact/Noise
Incorrect Interpretation of Signal
Insufficient Information
Inappropriate/Inadequate Shock/Stimulation
Premature Discharge of Battery
Fluid/Blood Leak; Mechanical Problem
Adverse Event Without Identified Device or Use Problem
Charging Problem
Adverse Event Without Identified Device or Use Problem
Failure to Seal
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Fluid/Blood Leak
Failure to Osseointegrate
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Device Handling Problem
Device Handling Problem
Device Handling Problem
Appropriate Term/Code Not Available
Device Handling Problem
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Device Handling Problem
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Battery Problem
Therapeutic or Diagnostic Output Failure
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Improper or Incorrect Procedure or Method
Detachment of Device or Device Component
Device Appears to Trigger Rejection
Infusion or Flow Problem