The following data is part of a premarket notification filed by Signus Medizintechnik Gmbh with the FDA for Kimba Mini.
| Device ID | K080349 |
| 510k Number | K080349 |
| Device Name: | KIMBA MINI |
| Classification | Spinal Vertebral Body Replacement Device |
| Applicant | SIGNUS MEDIZINTECHNIK GMBH 4050 OLSON MEMORIAL HWY SUITE 350 Minneapolis, MN 55422 |
| Contact | Alan Alexander |
| Correspondent | Alan Alexander SIGNUS MEDIZINTECHNIK GMBH 4050 OLSON MEMORIAL HWY SUITE 350 Minneapolis, MN 55422 |
| Product Code | MQP |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-02-11 |
| Decision Date | 2008-03-10 |
| Summary: | summary |