Epicardial Patch Lead
FDA premarket approval P900061/S158 · decided 2020-06-02
Approval details
- PMA number
- P900061
- Supplement
- S158
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- Epicardial Patch Lead
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2020-03-23
- Decision date
- 2020-06-02
- Days to decision
- 71 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Approval for a change to the lead serial number ink/foil material for select implantable leads.
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