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20,533 catalysts · 4,728 grant · 3,700 8k filing · 2,956 device 510k · 2,761 approval · 2,000 device pma · 2,000 device recall
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20,533 catalysts · 4,728 grant · 3,700 8k filing · 2,956 device 510k · 2,761 approval · 2,000 device pma · 2,000 device recall
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
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Improper Flow or 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
Obstruction of Flow
Fracture; Migration
Failure to Capture; Device Dislodged or Dislocated