K801010 is an FDA 510(k) clearance for the KIRSCHNER WIRE. This device is classified as a Rod, Fixation, Intramedullary And Accessories (Class II - Special Controls, product code HSB).
Submitted by American Safety Equipment Corp. (Mchenry, US). The FDA issued a Cleared decision on May 20, 1980, 22 days after receiving the submission on April 28, 1980.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3020.
| 510(k) Number | K801010 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 28, 1980 |
| Decision Date | May 20, 1980 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | HSB — Rod, Fixation, Intramedullary And Accessories |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3020 |