K041690 is an FDA 510(k) clearance for the MONARCH NASAL IMPLANT, a Prosthesis, Nose, Internal (Class II — Special Controls, product code FZE), submitted by Hanson Medical, Inc. (Kingston, US). The FDA issued a Cleared decision on February 11, 2005, 234 days after receiving the submission on June 22, 2004. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.3680.
| 510(k) Number | K041690 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 22, 2004 |
| Decision Date | February 11, 2005 |
| Days to Decision | 234 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FZE — Prosthesis, Nose, Internal |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.3680 |