Class Class II
PathLoc-TA Expandable Lumbar Cage System (K223474)
Description
PathLoc-TA Expandable Lumbar Cage System by L & K Biomed Co., Ltd., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223474
Clearance Date2023-01-13
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223474
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. PathLoc-TA Expandable Lumbar Cage System (K223474) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K221719 | ABTross ALIF Expandable Cage System | Aegis Spine, Inc. | 2022 |
Trace the full predicate network for K223474
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.