Class Class II
Sparrow Ascent (K251246)
Description
Sparrow Ascent by Spark Biomedical, Inc., an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251246
Clearance Date2025-08-25
Clearance TypeTraditional
Product CodePZR
Regulation Number882.5896
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251246
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. Sparrow Ascent (K251246) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233166 | NET Recovery Corp/NET Device | Net Recovery | 2024 |
| K230796 | Sparrow Ascent | Spark Biomedical, Inc. | 2023 |
Trace the full predicate network for K251246
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.