Class Class II
Extremity All Suture System (K241695)
Description
Extremity All Suture System by Field Orthopaedics, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241695
Clearance Date2024-09-12
Clearance TypeTraditional
Product CodeMBI
Regulation Number888.3040
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241695
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. Extremity All Suture System (K241695) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K180348 | Field Orthopaedics Micro Screw System | Field Orthopaedics Pty, Ltd. | 2018 |
| K151230 | Arthrex FiberTak Anchors | Arthrex, Inc. | 2015 |
| K112237 | MICROSUTURE ANCHORS | Arthrex, Inc. | 2011 |
Trace the full predicate network for K241695
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.