Class Class II
CORUS™ Navigation System-GX (K251060)
Description
CORUS™ Navigation System-GX by Providence Medical Technology, Inc., an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251060
Clearance Date2025-07-30
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251060
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. CORUS™ Navigation System-GX (K251060) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K240625 | CORUS Navigation Access System | Providence Medical Technology, Inc. | 2024 |
| K212636 | CORUS Spinal System-X | Providence Medical Technology, Inc. | 2021 |
| K191100 | ExcelsiusGPS Spine 1.1 Interbody Module | Globus Medical, Inc. | 2019 |
| K180876 | DTRAX Spinal System | Providence Medical Technology, Inc. | 2018 |
Trace the full predicate network for K251060
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.