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 |