K891599 is an FDA 510(k) clearance for the FILAFLEX ORTHODONTIC WIRE. This device is classified as a Bracket, Metal, Orthodontic (Class I - General Controls, product code EJF).
Submitted by American Orthodontics (Sheboygan, US). The FDA issued a Cleared decision on May 2, 1989, 43 days after receiving the submission on March 20, 1989.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.5410.
| 510(k) Number | K891599 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 20, 1989 |
| Decision Date | May 02, 1989 |
| Days to Decision | 43 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EJF — Bracket, Metal, Orthodontic |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.5410 |