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18,980 catalysts · 4,728 grant · 3,695 8k filing · 2,655 approval · 2,254 device 510k · 1,816 device recall · 1,567 device pma
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18,980 catalysts · 4,728 grant · 3,695 8k filing · 2,655 approval · 2,254 device 510k · 1,816 device recall · 1,567 device pma
Fracture; Migration
Failure to Capture; Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
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
Failure to Disconnect; Insufficient Information
Failure to Disconnect; Insufficient Information
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