Class Class II
Arthrex PushLock Suture Anchors (K251145)
Description
Arthrex PushLock Suture Anchors by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251145
Clearance Date2025-07-10
Clearance TypeTraditional
Product CodeMBI
Regulation Number888.3040
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251145
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. Arthrex PushLock Suture Anchors (K251145) cites 7 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K221099 | Arthrex Self-Punching PushLock Suture Anchor | Arthrex, Inc. | 2022 |
| K181513 | Arthrex PushLock Tenodesis Anchor | Arthrex, Inc. | 2018 |
| K151092 | Arthrex Short Suture Anchors | Arthrex, Inc. | 2016 |
| K101679 | ARTHREX PUSHLOCK ANCHORS | Arthrex, Inc. | 2010 |
| K093912 | ARTHREX TIBIAL GRAFTBOLT | Arthrex, Inc. | 2010 |
| K063479 | ARTHREX PUSHLOCK | Arthrex, Inc. | 2006 |
| K061863 | ARTHREX CORKSCREW SUTURE ANCHOR, TAK, AND PUSHLOCK FAMILY | Arthrex, Inc. | 2006 |
Trace the full predicate network for K251145
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.