Class Class II
NeuroBlate Fusion-S Software V3.17 (K222983)
Description
NeuroBlate Fusion-S Software V3.17 by Monteris Medical,, an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222983
Clearance Date2023-03-15
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222983
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. NeuroBlate Fusion-S Software V3.17 (K222983) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201056 | NeuroBlate System | Monteris Medical, Inc. | 2020 |
| K193375 | NeuroBlate System | Monteris Medical, | 2020 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K231061 | NeuroBlate System | Monteris Medical, | 2023 |
Trace the full predicate network for K222983
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.