SynchroMed Infusion System, SynchroMed II Infusion Pump
FDA premarket approval P860004/S281 · decided 2018-01-05
Approval details
- PMA number
- P860004
- Supplement
- S281
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- SynchroMed Infusion System, SynchroMed II Infusion Pump
- Generic name
- Pump, infusion, implanted, programmable
- Applicant
- Medtronic, Inc.
- Date received
- 2017-06-08
- Decision date
- 2018-01-05
- Days to decision
- 211 days
- Decision code
- APPR
- Product code
- LKK
- Advisory committee
- General Hospital
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Approval for the Model A810 SynchroMed II Clinician Programmer Application and Model 8880T2 Communicator intended for programming a SynchroMed II implantable infusion pump, and associated labeling and alarm changes.
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510(k) clearances by this applicant
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|---|---|---|
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| Retrograde Coronary Sinus Perfusion Cannulae (K253203) | Medtronic, Inc. | 2026-02-19 |
| Clearview Intracoronary Shunts (K253998) | Medtronic, Inc. | 2026-01-20 |
| Bio-Medicus Life Support Catheter and Introducer (K251831) | Medtronic, Inc. | 2026-01-15 |
| Concerto Versa™ Detachable Coil (K253511) | Medtronic, Inc. | 2026-01-14 |
| C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (K253409) | Medtronic, Inc. | 2025-12-19 |