calendar
19,335 catalysts · 4,728 grant · 3,674 8k filing · 2,674 approval · 2,394 device 510k · 1,898 device recall · 1,679 device pma
19,335 catalysts · 4,728 grant · 3,674 8k filing · 2,674 approval · 2,394 device 510k · 1,898 device recall · 1,679 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
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
Device Dislodged or Dislocated
Device Dislodged or Dislocated
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Improper Flow or 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
Obstruction of Flow
Fracture; Migration
Failure to Capture; 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
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Failure to Disconnect; Insufficient Information
Failure to Disconnect; Insufficient Information
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Premature Discharge of Battery
Migration
Insufficient Information
Loss of Osseointegration
Loss of Osseointegration
Unable to Obtain Readings; Device Displays Incorrect Message
Device Dislodged or Dislocated
High impedance; Capturing Problem
Adverse Event Without Identified Device or Use Problem