calendar
21,650 catalysts · 4,728 grant · 3,704 8k filing · 3,665 device 510k · 2,973 approval · 2,000 device pma · 2,000 device recall
next 91 dayslessmore
MonWedFri
21,650 catalysts · 4,728 grant · 3,704 8k filing · 3,665 device 510k · 2,973 approval · 2,000 device pma · 2,000 device recall
Insufficient Flow or Under Infusion
Failure to Capture; Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Fracture
Failure to Osseointegrate
Patient Device Interaction Problem
Loosening of Implant Not Related to Bone-Ingrowth
Migration
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Migration
Activation Failure
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Pumping Stopped
Adverse Event Without Identified Device or Use Problem
Failure to Read Input Signal
Priming 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
Wireless Communication 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
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