K810677 is an FDA 510(k) clearance for the MODELS 5976/5977 PACEMAKER PULSE GENER. This device is classified as a Implantable Pacemaker Pulse-generator (Class III - Premarket Approval, product code DXY).
Submitted by Medtronic, Inc. (Mounds View, US). The FDA issued a Cleared decision on May 27, 1981, 75 days after receiving the submission on March 13, 1981.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.3610.
| 510(k) Number | K810677 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 13, 1981 |
| Decision Date | May 27, 1981 |
| Days to Decision | 75 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DXY — Implantable Pacemaker Pulse-generator |
| Device Class | Class III - Premarket Approval |
| CFR Regulation | 21 CFR 870.3610 |