The following data is part of a premarket notification filed by Signus Medizintechnik Gmbh with the FDA for Nubic And Rabea Devices.
| Device ID | K082848 |
| 510k Number | K082848 |
| Device Name: | NUBIC AND RABEA DEVICES |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | SIGNUS MEDIZINTECHNIK GMBH 8202 SHERMAN ROAD Chseterland, OH 44026 |
| Contact | Karen E Warden |
| Correspondent | Karen E Warden SIGNUS MEDIZINTECHNIK GMBH 8202 SHERMAN ROAD Chseterland, OH 44026 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-09-29 |
| Decision Date | 2009-07-24 |
| Summary: | summary |