calendar
20,043 catalysts · 4,728 grant · 3,700 8k filing · 2,712 approval · 2,670 device 510k · 2,000 device recall · 1,887 device pma
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20,043 catalysts · 4,728 grant · 3,700 8k filing · 2,712 approval · 2,670 device 510k · 2,000 device recall · 1,887 device pma
Migration
Insufficient Information
Impedance Problem
Device Dislodged or Dislocated
Naturally Worn
Failure to Osseointegrate
Osseointegration Problem
Structural 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
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
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
Infusion or Flow Problem; Material Twisted/Bent
Patient Device Interaction Problem
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Malposition of Device
Device Dislodged or Dislocated
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Infusion or Flow Problem; Material Twisted/Bent
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Loss of or Failure to Bond; Premature Separation
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Material Separation
Adverse Event Without Identified Device or Use Problem
Use of Incorrect Control/Treatment Settings
Pumping Stopped
Adverse Event Without Identified Device or Use Problem