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18,630 catalysts · 4,728 grant · 3,686 8k filing · 2,621 approval · 2,129 device 510k · 1,725 device recall · 1,490 device pma
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18,630 catalysts · 4,728 grant · 3,686 8k filing · 2,621 approval · 2,129 device 510k · 1,725 device recall · 1,490 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
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