aprevo® anterior lumbar interbody fusion device with interfixation (K241477)
Description
aprevo® anterior lumbar interbody fusion device with interfixation by Carlsmed, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
FDA Database
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Predicate lineage for K241477
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. aprevo® anterior lumbar interbody fusion device with interfixation (K241477) cites 1 predicate device and is itself cited by 2 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222009 | aprevo® anterior lumbar interbody fusion device with interf... | Carlsmed, Inc. | 2022 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243802 | aprevo® anterior and lateral lumbar interbody fusion device... | Carlsmed, Inc. | 2025 |
| K243635 | aprevo® anterior lumbar interbody fusion device with interf... | Carlsmed, Inc. | 2024 |
Trace the full predicate network for K241477
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.