Class Class II
TACTIX Vector Syndesmosis System (K240035)
Description
TACTIX Vector Syndesmosis System by Vilex, LLC, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240035
Clearance Date2024-08-01
Clearance TypeTraditional
Product CodeHTN
Regulation Number888.3030
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240035
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. TACTIX Vector Syndesmosis System (K240035) cites 0 predicate devices and is itself cited by 1 later device.
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243408 | TACTIX Vector Syndesmosis System | Vilex, LLC | 2024 |
Trace the full predicate network for K240035
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.