Class Class II
Anovo Surgical System (model 6N) (K241907)
Description
Anovo Surgical System (model 6N) by Momentis Surgical , Ltd., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241907
Clearance Date2024-10-02
Clearance TypeTraditional
Product CodeQNM
Regulation Number878.4961
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241907
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. Anovo Surgical System (model 6N) (K241907) cites 1 predicate device and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232146 | Anovo Pedestal | Momentis Surgical , Ltd. | 2023 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K251761 | Anovo Surgical System (Model 6Ne); Anovo Instrument ARM Cur... | Momentis Surgical , Ltd. | 2025 |
Trace the full predicate network for K241907
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.