Class Class II
Trilogy Tissue Marker (K240429)
Description
Trilogy Tissue Marker by Inrad, Inc., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240429
Clearance Date2024-11-07
Clearance TypeTraditional
Product CodeNEU
Regulation Number878.4300
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240429
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. Trilogy Tissue Marker (K240429) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K183503 | EasyMark Tissue Marker | Inrad, Inc. | 2019 |
| K093256 | SELECTCORE VARIABLE THROW BIOPSY DEVICE MODEL 991014, 99151... | Inrad | 2009 |
Trace the full predicate network for K240429
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.