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21,841 catalysts · 4,728 grant · 3,778 device 510k · 3,712 8k filing · 3,032 approval · 2,000 device pma · 2,000 device recall
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21,841 catalysts · 4,728 grant · 3,778 device 510k · 3,712 8k filing · 3,032 approval · 2,000 device pma · 2,000 device recall
Charging Problem
Fluid/Blood Leak; Mechanical Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Premature Discharge of Battery
Unexpected Therapeutic Results
Nonstandard Device
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Charging 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
Adverse Event Without Identified Device or Use Problem
Positioning Failure
Adverse Event Without Identified Device or Use Problem
Positioning Failure
Firing Problem
Device Appears to Trigger Rejection
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Unintended Collision; Energy Output Problem
Device Stenosis
Key or Button Unresponsive/not Working
Insufficient Information
Positioning Failure
Use of Device Problem
Priming Problem
Adverse Event Without Identified Device or Use Problem
Use of Device Problem
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Loose or Intermittent Connection
Migration
Failure to Osseointegrate
Device Appears to Trigger Rejection
Insufficient Information
Failure to Advance; Deformation Due to Compressive Stress
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Disconnection; Pumping Stopped
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Material Rupture
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem