K251719
- 510(k) number
- K251719
- Device name
- Momentum® Posterior Spinal Fixation System
- Applicant
- Ulrich Medical USA, Inc. TX · US
- Product code
- NKB — Thoracolumbosacral Pedicle Screw System
- Decision date
- 2025-07-01
- Date received
- 2025-06-04
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K251719.pdf
Official FDA record: K251719
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.