Class Class II
Momentum® Posterior Spinal Fixation System (K251719)
Description
Momentum® Posterior Spinal Fixation System by Ulrich Medical USA, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251719
Clearance Date2025-07-01
Clearance TypeSpecial
Product CodeNKB
Regulation Number888.3070
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251719
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Momentum® Posterior Spinal Fixation System (K251719) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K231809 | Momentum® Posterior Spinal Fixation System with G21 V-STEAD... | Ulrich Medical USA | 2023 |
| K191932 | Momentum Posterior Spinal Fixation System | Ulrich Medical USA | 2019 |
| K180179 | Firebird® Spinal Fixation Systems: Firebird System; Firebir... | Orthofix, Inc. | 2018 |
Trace the full predicate network for K251719
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.