Class Class II
DePuy ATTUNE™ Total Knee System (K242665)
Description
DePuy ATTUNE™ Total Knee System by Depuy Orthopedics, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242665
Clearance Date2024-11-01
Clearance TypeTraditional
Product CodeOIY
Regulation Number888.3560
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242665
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. DePuy ATTUNE™ Total Knee System (K242665) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233980 | ATTUNE Total Knee System, ATTUNE Cementless Knee System, LP... | Depuy Ireland UC | 2024 |
| K201347 | DePuy ATTUNE Total Knee System | DePuy Orthopaedics, Inc. | 2020 |
| K103756 | DEPUY ATTUNE TOTAL KNEE SYSTEM | DePuy Orthopaedics, Inc. | 2011 |
| K101433 | DEPUY ATTUNE KNEE SYSTEM | DePuy Orthopaedics, Inc. | 2010 |
Trace the full predicate network for K242665
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.