K062821 is an FDA 510(k) clearance for the U-CLIP DEVICE. This device is classified as a Clip, Implantable (Class II - Special Controls, product code FZP).
Submitted by Medtronic Neurosurgery (Goleta, US). The FDA issued a Cleared decision on December 19, 2006, 90 days after receiving the submission on September 20, 2006.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4300.
| 510(k) Number | K062821 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 20, 2006 |
| Decision Date | December 19, 2006 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FZP — Clip, Implantable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4300 |