calendar
18,075 catalysts · 4,728 grant · 3,674 8k filing · 2,593 approval · 1,945 device 510k · 1,575 device recall · 1,351 device pma
18,075 catalysts · 4,728 grant · 3,674 8k filing · 2,593 approval · 1,945 device 510k · 1,575 device recall · 1,351 device pma
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
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
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Failure to Osseointegrate
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
Failure to Osseointegrate
Device Appears to Trigger Rejection
Insufficient Information
Failure to Osseointegrate
Migration
Insufficient Information
High impedance
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Material Rupture
Loosening of Implant Not Related to Bone-Ingrowth
Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
Failure to Osseointegrate
Positioning Failure
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Loosening of Implant Not Related to Bone-Ingrowth
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
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Over-Sensing
Material Rupture
Failure to Osseointegrate