K912764 is an FDA 510(k) clearance for the MEDTRONIC MODEL 3861 TEMPORARY SCREENING LEAD KIT. This device is classified as a Stimulator, Spinal-cord, Implanted (pain Relief) (Class II - Special Controls, product code GZB).
Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on November 22, 1991, 151 days after receiving the submission on June 24, 1991.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5880.
| 510(k) Number | K912764 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 24, 1991 |
| Decision Date | November 22, 1991 |
| Days to Decision | 151 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Statement |
| Product Code | GZB — Stimulator, Spinal-cord, Implanted (pain Relief) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5880 |