PMA P980016S961

Device: Cobalt MRI ICD (DDPB3D1, DDPB3D4, DVPB3D1, DVPB3D4); Cobalt XT MRI ICD (DDPA2D1, DDPA2D4, DVPA2D1, DVPA2D4); Crome MRI I
Applicant: Medtronic Cardiac Rhythm Disease Management
PMA number: P980016
Supplement: S961
Product code: LWS
Decision date: 2026-07-31
Classification: Cardiovascular
Generic name: Implantable cardioverter defibrillator (non-CRT)
Approval order statement: changes to cleaning process and revising acceptance criteria for final visual inspection of hybrid subassembly

Current openFDA PMA Record#

Device: Cobalt MRI ICD (DDPB3D1, DDPB3D4, DVPB3D1, DVPB3D4); Cobalt XT MRI ICD (DDPA2D1, DDPA2D4, DVPA2D1, DVPA2D4); Crome MRI I
Applicant: Medtronic Cardiac Rhythm Disease Management
PMA number: P980016
Supplement: S961
Product code: LWS
Generic name: Implantable cardioverter defibrillator (non-CRT)
Decision date: 2026-07-31
Decision code: OK30
Date received: 2026-07-07
Supplement type: 30-Day Notice
Supplement reason: Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement: changes to cleaning process and revising acceptance criteria for final visual inspection of hybrid subassembly