# K130089: Crosstrees Pva Pod

- Pathway: 510(k) (Traditional)
- Applicant: Crosstrees Medical, Inc.
- Decided: Aug 9, 2013 after 207 days
- Product code: NDN (Cement, Bone, Vertebroplasty)
- Device class: 2
- Regulation: 21 CFR 888.3027
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K100404 (2012). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100404: Ascendx VCF Reduction System, Aoi Medical, Inc. (2012) Summary page 2.

## Most influential descendants
- K133372: Crosstrees Pva Pod (2013), 0 descendants of its own

## Indications for use
The Crosstrees® PVA Pod device is intended to provide surgeons with a percutaneous means to deliver bone cement to painful pathologic compression fractures of the vertebral body in levels T4-L5 of the thoracic and lumbar spine. Pathologic fractures of the vertebral body may be caused by osteoporosis. It is intended to be used in combination with Crosstrees Fortibrae Bone Cement when delivered by the Crosstrees CDrive Bone Filler Delivery System.

Source page: https://510kreport.com/device/K130089
Methodology: https://510kreport.com/methodology