The following data is part of a premarket notification filed by Ulrich Medical Usa with the FDA for Momentum™ Posterior Spinal Fixation System.
| Device ID | K191932 | 
| 510k Number | K191932 | 
| Device Name: | Momentum™ Posterior Spinal Fixation System | 
| Classification | Thoracolumbosacral Pedicle Screw System | 
| Applicant | Ulrich Medical USA 5865 East State Rd.14 Chesterfield, MO 63005 | 
| Contact | Hans Stover | 
| Correspondent | Hans Stover Ulrich Medical USA 5865 East State Rd.14 Chesterfield, MO 63005 | 
| Product Code | NKB | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2019-07-19 | 
| Decision Date | 2019-10-02 |