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 |