K792311 is an FDA 510(k) clearance for the MEDTRONIC MODEL 7728 NEUROMOD. This device is classified as a Stimulator, Nerve, Transcutaneous, For Pain Relief (Class II - Special Controls, product code GZJ).
Submitted by Medtronic Vascular (Walker, US). The FDA issued a Cleared decision on November 21, 1979, 5 days after receiving the submission on November 16, 1979.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5890.
| 510(k) Number | K792311 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 16, 1979 |
| Decision Date | November 21, 1979 |
| Days to Decision | 5 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | — |
| Product Code | GZJ — Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5890 |