Class Class II
Arthrex Spine Endoscope (K243602)
Description
Arthrex Spine Endoscope by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243602
Clearance Date2025-05-16
Clearance TypeTraditional
Product CodeHRX
Regulation Number888.1100
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243602
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. Arthrex Spine Endoscope (K243602) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K130778 | DISCOSCOPES, CERVICAL ENDOSCOPES | Rz Medizintechnik GmbH | 2014 |
Trace the full predicate network for K243602
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.