calendar
7,606 catalysts · 3,431 8k filing · 1,096 grant · 1,000 device adverse event · 580 earnings · 550 approval · 430 device 510k
7,606 catalysts · 3,431 8k filing · 1,096 grant · 1,000 device adverse event · 580 earnings · 550 approval · 430 device 510k
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
Patient Device Interaction Problem
Failure to Osseointegrate
Patient-Device Incompatibility
Patient-Device Incompatibility
Patient-Device Incompatibility
Insufficient Information
Failure to Osseointegrate
Loss of Osseointegration
Electrical /Electronic Property Problem; Impedance Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Over-Sensing; Inappropriate/Inadequate Shock/Stimulation
Electrical /Electronic Property Problem; Under-Sensing
Material Rupture
Air/Gas in Device
Device Dislodged or Dislocated
Insufficient Information
Migration or Expulsion of Device
Use of Device Problem
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Use of Incorrect Control/Treatment Settings
Unintended Collision
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
Insufficient Information
Insufficient Information
Adverse Event Without Identified Device or Use Problem