PMA
P860004: MEDTRONIC(R) SYNCHROMED(TM) PUMP & INFUSION SYSTEM
FDA PMA · Pump, infusion, implanted, programmable · Medtronic, Inc.
Key facts
| PMA number | P860004 |
|---|---|
| Trade name | MEDTRONIC(R) SYNCHROMED(TM) PUMP & INFUSION SYSTEM |
| Generic name | Pump, infusion, implanted, programmable |
| Applicant | Medtronic, Inc. |
| Owner/operator | Medtronic, Inc. |
| Product code | LKK |
| Approval date | Mar 14, 1988 |
| Docket number | 88M-0114 |
| Notice date | May 11, 1988 |
| Establishment registration | 2182208 |
| FEI number | 2182208 |
At a glance
- 100–999 Supplements
- Aug 21, 2026 Latest supplement decision
- No Withdrawn
- No Summary of safety and effectiveness on file
- 100–999 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: