calendar
21,332 catalysts · 4,728 grant · 3,706 8k filing · 3,474 device 510k · 2,896 approval · 2,000 device pma · 2,000 device recall
21,332 catalysts · 4,728 grant · 3,706 8k filing · 3,474 device 510k · 2,896 approval · 2,000 device pma · 2,000 device recall
Insufficient Information
Failure to Osseointegrate
Migration
Insufficient Information
High impedance
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Material Rupture
Loosening of Implant Not Related to Bone-Ingrowth
Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
Failure to Osseointegrate
Positioning Failure
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Loosening of Implant Not Related to Bone-Ingrowth
Obstruction of Flow
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
Adverse Event Without Identified Device or Use Problem
Over-Sensing
Material Rupture
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Patient Device Interaction Problem
High impedance
Increase in Pressure
Positioning Failure
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Unraveled Material; Difficult to Advance
Off-Label Use; Material Puncture/Hole
Device Appears to Trigger Rejection
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Restricted Flow rate; Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Inflation Problem
Appropriate Term/Code Not Available
Device Appears to Trigger Rejection
Insufficient Information
Migration; Failure to Seal
Migration
Charging Problem
Fluid/Blood Leak; Mechanical Problem
Adverse Event Without Identified Device or Use Problem