# K072045: Oncontrol Bone Marrow Biopsy System

- Pathway: 510(k) (Traditional)
- Applicant: Vidacare Corporation
- Decided: Oct 22, 2007 after 89 days
- Product code: KNW (Instrument, Biopsy)
- Device class: 2
- Regulation: 21 CFR 876.1075
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K890925 (1989). 13 ancestors in all.
7 later devices descend from it; 3 cite it directly.
1 of 21 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062833: Powered EZ-IO Bone Marrow Aspiration System, Vidacare Corporation (2006) Summary page 1.
- K043523: Interv Brand Snarelok Bone Marrow Biopsy Needle, Medical Device Technologies, Inc. (2005) Summary page 2.
- K953064: Bioaccess Marrow Harvest System, Bioaccess, Inc. (1995) Summary page 1.

## Most influential descendants
- K081713: Vertebral Access System by Vidacare (2008), 4 descendants of its own
- K112468: The Oncontrol Bone Access System by Vidacare (2011), 3 descendants of its own
- K142377: The OnControl Bone Marrow Biopsy System by Vidacare (2014), 2 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

## Indications for use
The OnControlTM Bone Marrow Biopsy System is intended for bone marrow aspiration and biopsy.

Source page: https://510kreport.com/device/K072045
Methodology: https://510kreport.com/methodology