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18,639 catalysts · 4,728 grant · 3,695 8k filing · 2,621 approval · 2,129 device 510k · 1,725 device recall · 1,490 device pma
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18,639 catalysts · 4,728 grant · 3,695 8k filing · 2,621 approval · 2,129 device 510k · 1,725 device recall · 1,490 device pma
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
Loosening of Implant Not Related to Bone-Ingrowth
Adverse Event Without Identified Device or Use Problem