Class Class II
Talee, Talee PostOp (K241957)
Description
Talee, Talee PostOp by Invent Medical USA, LLC, an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241957
Clearance Date2024-08-30
Clearance TypeTraditional
Product CodeMVA
Regulation Number882.5970
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241957
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. Talee, Talee PostOp (K241957) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K230444 | Talee, Talee PostOp | Invent Medical USA, LLC | 2023 |
| K220681 | Talee, Talee PostOP | Invent Medical USA, LLC | 2022 |
Trace the full predicate network for K241957
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.