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14,971 catalysts · 3,606 8k filing · 2,670 grant · 2,420 approval · 1,702 device 510k · 1,263 device recall · 1,164 device pma
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14,971 catalysts · 3,606 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
Positioning Failure
Adverse Event Without Identified Device or Use Problem
Positioning Failure
Firing Problem
Device Appears to Trigger Rejection
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Unintended Collision; Energy Output Problem
Device Stenosis
Key or Button Unresponsive/not Working
Insufficient Information
Positioning Failure
Use of Device Problem
Priming Problem
Adverse Event Without Identified Device or Use Problem
Use of Device Problem
Adverse Event Without Identified Device or Use Problem
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Loose or Intermittent Connection
Migration
Failure to Osseointegrate
Device Appears to Trigger Rejection
Insufficient Information
Failure to Advance; Deformation Due to Compressive Stress
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Disconnection; Pumping Stopped
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Material Rupture
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Display or Visual Feedback Problem
Failure to Osseointegrate
Adverse Event Without Identified Device or Use Problem
Loss of Osseointegration
Failure to Osseointegrate
Insufficient Information
Loss of or Failure to Bond; Naturally Worn
Fracture
Adverse Event Without Identified Device or Use Problem
Device Alarm System
Unable to Obtain Readings; Device Displays Incorrect Message
Adverse Event Without Identified Device or Use Problem
Difficult to Fold, Unfold or Collapse; Patient-Device Incompatibility
High Readings