INTELLIS Adverse Event — Injury (MDR 3004209178-2020-07723)
INTELLIS Adverse Event — Injury (MDR 3004209178-2020-07723) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTELLIS; Generic name: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..
| Device | INTELLIS |
|---|---|
| Generic name | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07723 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | PRODUCT ID 977A260, SERIAL# (B)(4), IMPLANTED: (B)(6) 2019, EXPLANTED: (B)(6) 2020, PRODUCT TYPE: LEAD; PRODUCT ID: 977A275, SERIAL# (B)(4), IMPLANTED: (B)(6) 2019, EXPLANTED: (B)(6) 2020, PRODUCT TYPE: LEAD; PRODUCT ID: 977A260, SERIAL# (B)(4), IMPLANTED: (B)(6) 2019, EXPLANTED: (B)(6) 2020, PRODUCT TYPE: LEAD; PRODUCT ID: 97715, SERIAL# (B)(4), IMPLANTED: (B)(6) 2019, EXPLANTED: (B)(6) 2020, PRO |
| Source | openFDA MAUDE (device adverse events) |
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