TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System (K251502)
Description
TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System by Life Spine, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251502
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. TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System (K251502) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K221806 | TruLift Lateral Expandable Spacer System & Lateral Plate Sy... | Life Spine, Inc. | 2022 |
| K210061 | ProLift Lateral HELO Fixated | Life Spine, Inc. | 2021 |
| K202495 | SIRION Lateral Lumbar Interbody Fusion | Astura Medical, LLC | 2021 |
| K200338 | ProLift Lateral Fixated | Life Spine, Inc. | 2020 |
Trace the full predicate network for K251502
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.