Class Class II
Outlook Surgical Versa One System (8900139) (K241731)
Description
Outlook Surgical Versa One System (8900139) by Resnent, LLC, an FDA 510(k) cleared ear, nose, throat device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241731
Clearance Date2025-08-11
Clearance TypeTraditional
Product CodeEOB
Regulation Number874.4760
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241731
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. Outlook Surgical Versa One System (8900139) (K241731) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K191102 | Precision S 4K Sinuscope | Stryker | 2019 |
Trace the full predicate network for K241731
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.