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14,968 catalysts · 3,603 8k filing · 2,670 grant · 2,420 approval · 1,702 device 510k · 1,263 device recall · 1,164 device pma
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14,968 catalysts · 3,603 8k filing · 2,670 grant · 2,420 approval · 1,702 device 510k · 1,263 device recall · 1,164 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
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 Information
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
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Inappropriate/Inadequate Shock/Stimulation; Migration
Inappropriate/Inadequate Shock/Stimulation; Migration
Loosening of Implant Not Related to Bone-Ingrowth
Adverse Event Without Identified Device or Use Problem
Wireless Communication Problem
Fracture
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
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
Failure to Advance
Adverse Event Without Identified Device or Use Problem
Electrical /Electronic Property Problem; Under-Sensing
Leak/Splash
Adverse Event Without Identified Device or Use Problem
Leak/Splash
Leak/Splash
Leak/Splash
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Patient Device Interaction Problem
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem