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7,557 catalysts · 3,382 8k filing · 1,096 grant · 1,000 device adverse event · 580 earnings · 550 approval · 430 device 510k
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7,557 catalysts · 3,382 8k filing · 1,096 grant · 1,000 device adverse event · 580 earnings · 550 approval · 430 device 510k
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Premature Discharge of Battery
Migration
Insufficient Information
Loss of Osseointegration
Loss of Osseointegration
Unable to Obtain Readings; Device Displays Incorrect Message
Device Dislodged or Dislocated
High impedance; Capturing Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Pacing Problem; Unexpected Therapeutic Results
Adverse Event Without Identified Device or Use Problem
Fracture
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