K090679 is an FDA 510(k) clearance for the VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM. This device is classified as a Device, Anastomotic, Microvascular (Class II - Special Controls, product code MVR).
Submitted by Vioptix, Inc. (Irvine, US). The FDA issued a Cleared decision on April 17, 2009, 32 days after receiving the submission on March 16, 2009.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4300.
| 510(k) Number | K090679 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 16, 2009 |
| Decision Date | April 17, 2009 |
| Days to Decision | 32 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | MVR — Device, Anastomotic, Microvascular |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4300 |