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17,817 catalysts · 4,639 grant · 3,674 8k filing · 2,587 approval · 1,903 device 510k · 1,500 device recall · 1,315 device pma
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17,817 catalysts · 4,639 grant · 3,674 8k filing · 2,587 approval · 1,903 device 510k · 1,500 device recall · 1,315 device pma
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
Loosening of Implant Not Related to Bone-Ingrowth
Improper or Incorrect Procedure or Method
Loosening of Implant Not Related to Bone-Ingrowth
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Over-Sensing
Adverse Event Without Identified Device or Use Problem
Fluid/Blood Leak
Failure to Osseointegrate
Fluid/Blood Leak
Therapeutic or Diagnostic Output Failure
Adverse Event Without Identified Device or Use Problem
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
Pumping Stopped
Adverse Event Without Identified Device or Use Problem