The following data is part of a premarket notification filed by Ulrich Gmbh & Co. Kg with the FDA for Ucentum.
| Device ID | K123717 | 
| 510k Number | K123717 | 
| Device Name: | UCENTUM | 
| Classification | Thoracolumbosacral Pedicle Screw System | 
| Applicant | ULRICH GMBH & CO. KG 612 TRADE CENTER BLVD Chesterfield, MO 63005 | 
| Contact | Hans Stover | 
| Correspondent | Hans Stover ULRICH GMBH & CO. KG 612 TRADE CENTER BLVD Chesterfield, MO 63005 | 
| Product Code | NKB | 
| Subsequent Product Code | MNH | 
| Subsequent Product Code | MNI | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Se - With Limitations (SESU) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2012-12-04 | 
| Decision Date | 2013-03-04 | 
| Summary: | summary | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  UCENTUM  79098683  4181295 Live/Registered | Ulrich GmbH & Co. KG 2011-05-31 |