The following data is part of a premarket notification filed by Signus Medizintechnik Gmbh with the FDA for Mobis, Moval, Semial, Tetrismodel Peek And Titanium, Kimba Model Standard And Mini.
| Device ID | K111792 |
| 510k Number | K111792 |
| Device Name: | MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | SIGNUS MEDIZINTECHNIK GMBH 8202 SHERMAN ROAD Chesterland, OH 44026 -2141 |
| Contact | Karen E Warden, Phd |
| Correspondent | Karen E Warden, Phd SIGNUS MEDIZINTECHNIK GMBH 8202 SHERMAN ROAD Chesterland, OH 44026 -2141 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-06-27 |
| Decision Date | 2012-03-05 |
| Summary: | summary |