Class Class II
Freedom Posterior Cervical Screws (K242674)
Description
Freedom Posterior Cervical Screws by Signature Orthopaedics Pty, Ltd., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242674
Clearance Date2025-05-13
Clearance TypeTraditional
Product CodeNKG
Regulation Number888.3075
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242674
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. Freedom Posterior Cervical Screws (K242674) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K182508 | Saxxony™ Posterior Cervical Thoracic System | Nexxt Spine, LLC | 2018 |
Trace the full predicate network for K242674
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.