The following data is part of a premarket notification filed by Medtronic Inc.,neurological Division with the FDA for Model 3873 1* 8 And Model 3874 1* 8 Compact Test Stimulation Leads.
| Device ID | K051773 |
| 510k Number | K051773 |
| Device Name: | MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS |
| Classification | Stimulator, Spinal-cord, Implanted (pain Relief) |
| Applicant | MEDTRONIC INC.,NEUROLOGICAL DIVISION 710 MEDTRONIC PKWY. Minneapolis, MN 55432 |
| Contact | Paula Cordero |
| Correspondent | Paula Cordero MEDTRONIC INC.,NEUROLOGICAL DIVISION 710 MEDTRONIC PKWY. Minneapolis, MN 55432 |
| Product Code | GZB |
| CFR Regulation Number | 882.5880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-07-01 |
| Decision Date | 2005-07-28 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00613994756688 | K051773 | 000 |
| 00613994756664 | K051773 | 000 |
| 00613994756640 | K051773 | 000 |
| 00613994756626 | K051773 | 000 |
| 00643169157415 | K051773 | 000 |
| 00643169157392 | K051773 | 000 |
| 00643169157385 | K051773 | 000 |
| 00643169157361 | K051773 | 000 |