Class Class II
Arthrex VAL and VAL KreuLock™ Compression Screw System (K242554)
Description
Arthrex VAL and VAL KreuLock™ Compression Screw System by Arthrex, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242554
Clearance Date2024-10-21
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242554
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 VAL and VAL KreuLock™ Compression Screw System (K242554) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K220937 | Arthrex Mini Fragment System | Arthrex, Inc. | 2022 |
| K203294 | Arthrex Pilon Fusion System | Arthrex, Inc. | 2021 |
| K201132 | Arthrex Compression Screws | Arthrex, Inc. | 2020 |
| K103705 | LOW PROFILE SCREWS | Arthrex, Inc. | 2011 |
| K082516 | PERI-LOC PERIARTICULAR LOCKED PLATING SYSTEM HEXALOBULAR BO... | Smith & Nephew, Inc. | 2008 |
Trace the full predicate network for K242554
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.