calendar
13,363 catalysts · 3,603 8k filing · 2,401 grant · 2,054 approval · 1,400 device 510k · 1,000 device adverse event · 944 device recall
next 91 dayslessmore
MonWedFri
13,363 catalysts · 3,603 8k filing · 2,401 grant · 2,054 approval · 1,400 device 510k · 1,000 device adverse event · 944 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