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 |