Class Class II
Xenco Medical CancelleX Cervical Interbody System (K243673)
Description
Xenco Medical CancelleX Cervical Interbody System by Xenco Medical, LLC, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243673
Clearance Date2025-01-29
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243673
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. Xenco Medical CancelleX Cervical Interbody System (K243673) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222015 | Integral Titanium Cervical Interbody | Nvision Biomedical Technologies, Inc. | 2023 |
| K140786 | XENCO MEDICAL CERVICAL INTERBODY SYSTEM | Xenco Medical, LLC | 2014 |
Trace the full predicate network for K243673
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.