Class Class II
ProLift Micro Expandable Spacer System (K223430)
Description
ProLift Micro Expandable Spacer System by Life Spine, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223430
Clearance Date2023-05-04
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223430
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. ProLift Micro Expandable Spacer System (K223430) cites 0 predicate devices and is itself cited by 3 later devices.
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K250373 | ProLift Expandable Spacer System | Life Spine, Inc. | 2025 |
| K243668 | ProLift Pivot Expandable Spacer System | Life Spine, Inc. | 2025 |
| K232611 | TruLift Micro Expandable Spacer System & TruLift Expandable... | Life Spine, Inc. | 2023 |
Trace the full predicate network for K223430
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.