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 |