# K081713: Vertebral Access System by Vidacare

- Pathway: 510(k) (Traditional)
- Applicant: Vidacare Corporation
- Decided: Nov 21, 2008 after 157 days
- Product code: MOQ (Battery, Replacement, Rechargeable)
- Device class: 1
- Regulation: 21 CFR 878.4820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K890925 (1989). 15 ancestors in all.
4 later devices descend from it; 1 cites it directly.
1 of 20 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072045: Oncontrol Bone Marrow Biopsy System, Vidacare Corporation (2007) Summary page 2.
- K051820: Parallax Ezflow Cement Delivery System, Arthrocare Corp. (2005) Summary page 2.

## Most influential descendants
- K112468: The Oncontrol Bone Access System by Vidacare (2011), 3 descendants of its own
- K113872: The Oncontrol Bone Access and Bone Biopsy System by Vidacare (2012), 2 descendants of its own
- K230015: OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver (2023), 0 descendants of its own
- K213896: BD Trek Powered Bone Biopsy System (2022), 0 descendants of its own

## Indications for use
The Vertebral Access System by Vidacare® is intended for use with a standard cement delivery system for the fixation of fractures of the vertebral body using vertebroplasty. This system does not contain cement.

Source page: https://510kreport.com/device/K081713
Methodology: https://510kreport.com/methodology