Class Class II
SpineSite Endoscope System (K241990)
Description
SpineSite Endoscope System by Hydrocision, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241990
Clearance Date2025-07-30
Clearance TypeTraditional
Product CodeHRX
Regulation Number888.1100
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241990
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. SpineSite Endoscope System (K241990) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201134 | Arthrex NanoScope System | Arthrex, Inc. | 2020 |
Trace the full predicate network for K241990
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.