K801310 is an FDA 510(k) clearance for the THE MAGTEC SYSTEM..
Submitted by Valley Forge Scientific Corp. (Mchenry, US). The FDA issued a Cleared decision on June 20, 1980, 17 days after receiving the submission on June 3, 1980.
This device falls under the General & Plastic Surgery FDA review panel.
| 510(k) Number | K801310 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 03, 1980 |
| Decision Date | June 20, 1980 |
| Days to Decision | 17 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | — |
| Device Class | — |