K915540 is an FDA 510(k) clearance for the MODEL 3587A RESUME II LEAD. This device is classified as a Stimulator, Peripheral Nerve, Implanted (pain Relief) (Class II - Special Controls, product code GZF).
Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on January 22, 1992, 43 days after receiving the submission on December 10, 1991.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5870.
| 510(k) Number | K915540 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 10, 1991 |
| Decision Date | January 22, 1992 |
| Days to Decision | 43 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Statement |
| Product Code | GZF — Stimulator, Peripheral Nerve, Implanted (pain Relief) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5870 |