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13,623 catalysts · 3,603 8k filing · 2,401 grant · 2,100 approval · 1,445 device 510k · 1,074 device recall · 1,000 device adverse event
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13,623 catalysts · 3,603 8k filing · 2,401 grant · 2,100 approval · 1,445 device 510k · 1,074 device recall · 1,000 device adverse event
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
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