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 |