Activa Deep Brain Stimulation Therapy System
FDA premarket approval P960009/S322 · decided 2019-06-14
Approval details
- PMA number
- P960009
- Supplement
- S322
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Activa Deep Brain Stimulation Therapy System
- Generic name
- Stimulator, electrical, implanted, for parkinsonian tremor
- Applicant
- Medtronic, Inc.
- Date received
- 2018-08-08
- Decision date
- 2019-06-14
- Days to decision
- 310 days
- Decision code
- APPR
- Product code
- MHY
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Approval for a change in the external supplier lithium source and an addition of a lithium purification process step.
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