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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
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
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
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Device Appears to Trigger Rejection
Intermittent Capture; High Capture Threshold
Patient Device Interaction Problem
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Failure to Interrogate; Communication or Transmission Problem
Detachment of Device or Device Component
Expulsion
Expulsion
Obstruction of Flow
Patient-Device Incompatibility
Patient-Device Incompatibility
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Signal Artifact/Noise; Electromagnetic Interference
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
Signal Artifact/Noise; Fracture
Patient Device Interaction Problem
Patient Device Interaction Problem
Material Rupture
Difficult to Remove
Insufficient Flow or Under Infusion
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
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
Device Appears to Trigger Rejection
Insufficient Flow or Under Infusion
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Wireless Communication Problem