CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant (K251885)
Description
CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant by Providence Medical Technology, Inc., an FDA 510(k) cleared unknown device.
Regulatory Information
FDA Database
View on FDA DatabasePredicate lineage for K251885
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. CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant (K251885) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241035 | PMT Posterior Cervical Stabilization System (PCSS) | Providence Medical Technology, Inc. | 2024 |
| K230840 | PMT Facet Fixation System, Lumbar (PMT FFS-LX) | Providence Medical Technology, Inc. | 2023 |
| K220951 | PMT Facet Fixation System (PMT FFS) | Providence Medical Technology, Inc. | 2022 |
Trace the full predicate network for K251885
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.