# K133328: Aero-AL Lumbar Cage System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corporation
- Decided: May 30, 2014 after 213 days
- Product code: OVD (Intervertebral Fusion Device With Integrated Fixation, Lumbar)
- Device class: 2
- Regulation: 21 CFR 888.3080
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
638 later devices descend from it; 2 cite it directly.
0 of 639 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K143163: AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK Spacer, AVS® Navigator PEEK Spacer, AVS® ARIA PEEK Spacer, AccuLIF TL and PL Cage, AVS® Anchor-L Spacer, Aero-AL Lumbar Cage System (2015), 636 descendants of its own
- K143616: AccuLIF TL and PL Cage (2015), 469 descendants of its own
- K152304: Tritanium PL Cage (2015), 448 descendants of its own
- K153782: NuVasive® Lumbar Interbody Implants (2016), 390 descendants of its own
- K161230: NuVasive Lumbar Interbody Implants (2016), 381 descendants of its own

Source page: https://510kreport.com/device/K133328
Methodology: https://510kreport.com/methodology