Class Class U
Arthrex Spine Compression FT Screw (K250920)
Description
Arthrex Spine Compression FT Screw by Arthrex, Inc., an FDA 510(k) cleared unknown device.
Regulatory Information
Device ClassClass Class U
510(k) NumberK250920
Clearance Date2025-05-22
Clearance TypeTraditional
Product CodeMRW
FDA Database
View on FDA DatabasePredicate lineage for K250920
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 Spine Compression FT Screw (K250920) cites 6 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201132 | Arthrex Compression Screws | Arthrex, Inc. | 2020 |
| K192744 | CORRIDOR Fixation System | Globus Medical, Inc. | 2019 |
| K182361 | Arthrex Compression FT Screws | Arthrex, Inc. | 2018 |
| K170382 | Arthrex Compression Screws | Arthrex, Inc. | 2017 |
| K150456 | Arthrex Plates, Screws, and Staples | Arthrex, Inc. | 2015 |
| K132217 | ARTHREX COMPRESSION FT SCREWS | Arthrex, Inc. | 2013 |
Trace the full predicate network for K250920
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.