Cobalt MRI ICD, Cobalt XT MRI ICD, Srome MRI ICD
FDA premarket approval P980016/S932 · decided 2025-08-12
Approval details
- PMA number
- P980016
- Supplement
- S932
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Cobalt MRI ICD, Cobalt XT MRI ICD, Srome MRI ICD
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2025-07-17
- Decision date
- 2025-08-12
- Days to decision
- 26 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- a supplier update to their wafer polishing washing process, new equivalent equipment, and a duplicate cleaning step in the manufacturing process flow
Class III intelligence, same tools
PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.