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20,043 catalysts · 4,728 grant · 3,700 8k filing · 2,712 approval · 2,670 device 510k · 2,000 device recall · 1,887 device pma
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20,043 catalysts · 4,728 grant · 3,700 8k filing · 2,712 approval · 2,670 device 510k · 2,000 device recall · 1,887 device pma
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Insufficient Flow or Under Infusion
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Capture; Device Sensing 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
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
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
Adverse Event Without Identified Device or Use Problem
Battery Problem; Power Problem
Adverse Event Without Identified Device or Use Problem
Material Rupture
Wireless Communication Problem
Adverse Event Without Identified Device or Use Problem; Appropriate Term/Code Not Available
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
Device Appears to Trigger Rejection
Device Appears to Trigger Rejection
Device Appears to Trigger Rejection
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Device Appears to Trigger Rejection
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Loosening of Implant Not Related to Bone-Ingrowth
Device Appears to Trigger Rejection
Implant subsidence
Osseointegration Problem
Device Dislodged or Dislocated