Class Class II
VIA360™ Surgical System (K243503)
Description
VIA360™ Surgical System by New World Medical, Inc., an FDA 510(k) cleared general hospital device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243503
Clearance Date2025-02-14
Clearance TypeTraditional
Product CodeMRH
Regulation Number880.5725
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243503
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. VIA360™ Surgical System (K243503) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K173332 | OMNI Surgical System | Sight Sciences, Inc. | 2017 |
Trace the full predicate network for K243503
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.